Reaction #4117485
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1c530c4ad79b4f2eb639f34eb0f5d03dNo renderable structure data available
C1=CC=C(C(=C1)F)SC(F)(F)FChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 1-fluoro-2-(trifluoromethylsulfanyl)benzene |
|---|---|
| IUPAC Name | — |
| CAS Number | 1978-16-1 |
| Database ID | 47002880 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
1-fluoro-2-(trifluoromethylsulfanyl)benzene (CAS 1978-16-1) 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 47002880
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-1c530c4ad79b4f2eb639f34eb0f5d03dConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-e5991bfa76b94b27be2b99a7db65ab37Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-e5991bfa76b94b27be2b99a7db65ab37Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-ebb48609c819406090fe9802aa4af027Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-ebb48609c819406090fe9802aa4af027Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-eb20db125d304f47aba3502b0deb2fb1Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-ec467a4372804a8b94ec7fe1ca4179e8Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M aqueous NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-720bceb42ff6432cace14bcbaefbb80dConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1c530c4ad79b4f2eb639f34eb0f5d03dConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-ea72c56fff8e40d995be2c5f5e9d3af7Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-29aa01dbf5b6404a87c06fc66cab0539Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Methyl viologen hydrochloride (1.17 g) in N,N-dimethylformamide (80 mL) at 25° C. was saturated with trifluoromethyl iodide, treated with 2-fluorobenzenethiol (9.7 mL) and triethylamine (20 mL), stirred for 24 hours, diluted with water (240 mL) and extracted with diethyl ether. The extract was washed with 1M NaOH, saturated ammonium chloride and brine and concentrated. at 25° C. extracted with diethyl ether The extract was washed with 1M NaOH, saturated ammonium chloride and brine concentrated
Source ID: ord-2844b581592343e69d559dcd180f37c1PubChem References
These sources are listed in the compound's public database record.
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