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COC(=O)CSC(=S)C1=CC=CC=C1Chemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | methyl 2-(benzenecarbonothioylsulfanyl)acetate |
|---|---|
| IUPAC Name | — |
| CAS Number | 27249-65-6 |
| Database ID | 71356278 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
methyl 2-(benzenecarbonothioylsulfanyl)acetate (CAS 27249-65-6) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 71356278
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-87bf97f79a8343f29b05d65253c18155Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid methyl ester (1.9 g, 8.4 mmol) in ethanol (30 mL) to a solution of anhydrous hydrazine (1 mL) at room temperature under nitrogen and stir for 2 hours. Then add water (20 mL) and remove the solvent under reduced pressure. Dissolve the residue in ethyl acetate (300 mL), wash with water (200 mL) and brine (200 mL), and dry over magnesium sulfate. Remove the solvent under reduced pressure to provide thiobenzoic acid hydrazide (1.2 g, 94%). Then add water (20 mL) and remove the solvent under reduced pressure Dissolve the residue in ethyl acetate (300 mL) wash with water (200 mL) and brine (200 mL) dry over magnesium sulfate Remove the solvent under reduced pressure
Source ID: ord-e4fcfebd8f5843d19cbaa5f7df69b2d0Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid methyl ester (1.9 g, 8.4 mmol) in ethanol (30 mL) to a solution of anhydrous hydrazine (1 mL) at room temperature under nitrogen and stir for 2 hours. Then add water (20 mL) and remove the solvent under reduced pressure. Dissolve the residue in ethyl acetate (300 mL), wash with water (200 mL) and brine (200 mL), and dry over magnesium sulfate. Remove the solvent under reduced pressure to provide thiobenzoic acid hydrazide (1.2 g, 94%). Then add water (20 mL) and remove the solvent under reduced pressure Dissolve the residue in ethyl acetate (300 mL) wash with water (200 mL) and brine (200 mL) dry over magnesium sulfate Remove the solvent under reduced pressure
Source ID: ord-e4fcfebd8f5843d19cbaa5f7df69b2d0Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid (5.5 g, 26.0 mmol) in methanol (100 mL) and to a solution of thionyl chloride (52 mL) at room temperature under nitrogen and heat the mixture at reflux for 12 hours. Remove the solvent under reduced pressure, dissolve the residue in ethyl acetate (200 mL), wash with saturated NaHCO3 (200 mL) and brine (200 mL) solutions, and dry over sodium sulfate. Remove the solvent under reduced pressure to provide thiobenzoylsulfanylacetic acid methyl ester (5.7 g, 97%). at reflux for 12 hours Remove the solvent under reduced pressure dissolve the residue in ethyl acetate (200 mL) wash with saturated NaHCO3 (200 mL) and brine (200 mL) solutions dry over sodium sulfate Remove the solvent under reduced pressure
Source ID: ord-688984c870574770a6a80db22151b732Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-87bf97f79a8343f29b05d65253c18155Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl 2-((phenylcarbonothioyl)thio)acetate (3.6 g, 15.9 mmol) and 3-amino-6-bromopyrazine-2-carbohydrazide (2.9 g, 12.5 mmol) were suspended in 200 mL of ethanol and refluxed for 2 days. To the mixture, 50 mL of sat. ethanolic HCl was added and the mixture was refluxed overnight. A precipitate formed. The formed solid was filtered and dried to afford 5-Bromo-3-(5-phenyl-1,3,4-thiadiazol-2-yl)pyrazin-2-amine 5 (1.5 g, 36%). refluxed for 2 days the mixture was refluxed overnight A precipitate formed The formed solid was filtered dried
Source ID: ord-2cbc8a8a228140bbba6a6dbcefb60f77Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 2-((Phenylcarbonothioyl)thio)acetic acid (10 g, 47.1 mmol) was dissolved in 200 mL of methanol followed by the dropwise addition of thionylchloride (16 g, 120 mmol) at room temperature. The reaction mixture was refluxed for 4 hours. The reaction mixture was concentrated in vacuo and ethyl acetate was added. The mixture was washed with sat. aq. NaHCO3 and brine and dried over Na2SO4. The reaction mixture was concentrated in vacuo to afford Methyl 2-((phenylcarbonothioyl)thio)acetate 2 as brown oil (10.5 g, 98%). The reaction mixture was refluxed for 4 hours The reaction mixture was concentrated in vacuo and ethyl acetate was added The mixture was washed with sat. aq. NaHCO3 and brine dried over Na2SO4 The reaction mixture was concentrated in vacuo
Source ID: ord-d3aef15bfca74418ab7803638a34a11dConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid methyl ester (1.9 g, 8.4 mmol) in ethanol (30 mL) to a solution of anhydrous hydrazine (1 mL) at room temperature under nitrogen and stir for 2 hours. Then add water (20 mL) and remove the solvent under reduced pressure. Dissolve the residue in ethyl acetate (300 mL), wash with water (200 mL) and brine (200 mL), and dry over magnesium sulfate. Remove the solvent under reduced pressure to provide thiobenzoic acid hydrazide (1.2 g, 94%). Then add water (20 mL) and remove the solvent under reduced pressure Dissolve the residue in ethyl acetate (300 mL) wash with water (200 mL) and brine (200 mL) dry over magnesium sulfate Remove the solvent under reduced pressure
Source ID: ord-ba5d82d32f0e4da5af7db1d74368ee13Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid (5.5 g, 26.0 mmol) in methanol (100 mL) and to a solution of thionyl chloride (52 mL) at room temperature under nitrogen and heat the mixture at reflux for 12 hours. Remove the solvent under reduced pressure, dissolve the residue in ethyl acetate (200 mL), wash with saturated NaHCO3 (200 mL) and brine (200 mL) solutions, and dry over sodium sulfate. Remove the solvent under reduced pressure to provide thiobenzoylsulfanylacetic acid methyl ester (5.7 g, 97%). at reflux for 12 hours Remove the solvent under reduced pressure dissolve the residue in ethyl acetate (200 mL) wash with saturated NaHCO3 (200 mL) and brine (200 mL) solutions dry over sodium sulfate Remove the solvent under reduced pressure
Source ID: ord-44090259540147818b7e3f401aec688eConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid methyl ester (1.9 g, 8.4 mmol) in ethanol (30 mL) to a solution of anhydrous hydrazine (1 mL) at room temperature under nitrogen and stir for 2 hours. Then add water (20 mL) and remove the solvent under reduced pressure. Dissolve the residue in ethyl acetate (300 mL), wash with water (200 mL) and brine (200 mL), and dry over magnesium sulfate. Remove the solvent under reduced pressure to provide thiobenzoic acid hydrazide (1.2 g, 94%). Then add water (20 mL) and remove the solvent under reduced pressure Dissolve the residue in ethyl acetate (300 mL) wash with water (200 mL) and brine (200 mL) dry over magnesium sulfate Remove the solvent under reduced pressure
Source ID: ord-643fe99d9aef4473a01d8af06d2d8ee8Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid (5.5 g, 26.0 mmol) in methanol (100 mL) and to a solution of thionyl chloride (52 mL) at room temperature under nitrogen and heat the mixture at reflux for 12 hours. Remove the solvent under reduced pressure, dissolve the residue in ethyl acetate (200 mL), wash with saturated NaHCO3 (200 mL) and brine (200 mL) solutions, and dry over sodium sulfate. Remove the solvent under reduced pressure to provide thiobenzoylsulfanylacetic acid methyl ester (5.7 g, 97%). at reflux for 12 hours Remove the solvent under reduced pressure dissolve the residue in ethyl acetate (200 mL) wash with saturated NaHCO3 (200 mL) and brine (200 mL) solutions dry over sodium sulfate Remove the solvent under reduced pressure
Source ID: ord-ed9ca21e57664f439c324c19bebe20e4Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Add a solution of thiobenzoylsulfanylacetic acid methyl ester (1.9 g, 8.4 mmol) in ethanol (30 mL) to a solution of anhydrous hydrazine (1 mL) at room temperature under nitrogen and stir for 2 hours. Then add water (20 mL) and remove the solvent under reduced pressure. Dissolve the residue in ethyl acetate (300 mL), wash with water (200 mL) and brine (200 mL), and dry over magnesium sulfate. Remove the solvent under reduced pressure to provide thiobenzoic acid hydrazide (1.2 g, 94%). Then add water (20 mL) and remove the solvent under reduced pressure Dissolve the residue in ethyl acetate (300 mL) wash with water (200 mL) and brine (200 mL) dry over magnesium sulfate Remove the solvent under reduced pressure
Source ID: ord-e4fcfebd8f5843d19cbaa5f7df69b2d0PubChem References
These sources are listed in the compound's public database record.
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