Reaction #4168350
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1747d6eb4f594a91ba18d61c5bc1d314No renderable structure data available
CC1=C(C(=CC=C1)Cl)NChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 2-chloro-6-methylaniline |
|---|---|
| IUPAC Name | — |
| CAS Number | 87-63-8 |
| Database ID | 6897 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
2-chloro-6-methylaniline (CAS 87-63-8) 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 6897
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-1747d6eb4f594a91ba18d61c5bc1d314Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2ef70e822941461a8426e5277efdae27Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-05377de3043546988f4ae1f5ce95abd7Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-92ce3c7961ed413187ebfa5af0096141Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ea10b5eb72704d1c898486b5ed1d556eConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ee7954c1f5064386ace3158d762215f4Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c869de14804c46189f65d8dd38181291Conditions: temp:7.51; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 2-chloro-6-methyl-phenylamine (500 mg, 3.53 mmol) m H2SO4 (1.37 mL) was diluted by adding over 15 min 2 mL of water in order to maintain a temperature below 90° C. Then the reaction mixture was cooled to 5-10° C. and a solution of sodium nitrite (246 mg, 3.57 mmol) in water (1 mL) was added over 2 hours. The resulting diazonium solution was then added to a solution of sodium acetate (5.21 g, 63.6 mmol) in water (20 mL) at a temperature maintained between 65 to 75° C. The resulting precipitate with filtered and treated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100. The aqueous phase was separated while hot from the small amount of black tarry by-products, cooled to 50-6° C. and acidified with HCl (37%, 12.5 mL). The reaction mixture was cooled down to room temperature, the resulting precipitate was filtered, was washed thrice with cold water and was dried under vacuum to yield 7-chloro-1H-indazole (220 mg, 1.44 mmol, 41%) as a white solid. to maintain a temperature below 90° C maintained between 65 to 75° C The resulting precipitate with filtered treated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100 The aqueous phase was separated while hot from the small amount of black tarry by-products cooled to 50-6° C. The reaction mixture was cooled down to room temperature the resulting precipitate was filtered was washed thrice with cold water was dried under vacuum
Source ID: ord-0b895c720cf94b4c9cbfbee5dd2e3a55Conditions: temp:7.51; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 2-chloro-6-methyl-phenylamine (500 mg, 3.53 mmol) in H2SO4 (1.37 mL) was diluted by adding over 15 min. 2 mL of water in order to maintain a temperature below 90° C. Then the reaction mixture was cooled to 5-10° C. and a solution of sodium nitrite (246 mg, 3.57 mmol) in water (1 mL) was added over 2 hours. The resulting diazonium solution was then added to a solution of sodium acetate (5.21 g, 63.6 mmol) in water (20 mL) at a temperature maintained between 65 to 75° C. The resulting precipitate was filtered and treated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100° C. The aqueous phase was separated while hot from the small amount of black tarry by-products, cooled to 50-60° C. and acidified with HCl (37%, 12.5 mL). The reaction mixture was cooled down to room temperature, the resulting precipitate was filtered, was washed thrice with cold water and was dried under vacuum to yield 7-chloro-1H-indazole (220 mg, 1.44 mmol, 41%) as a white solid. by adding over 15 min maintained between 65 to 75° C The resulting precipitate was filtered treated with a solution of NaOH (6.00 g) in water (100 mL) at 95-100° C The aqueous phase was separated while hot from the small amount of black tarry by-products cooled to 50-60° C. The reaction mixture was cooled down to room temperature the resulting precipitate was filtered was washed thrice with cold water was dried under vacuum
Source ID: ord-c8ae5b2e49c64cb1bd87c65406178cfaConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-1747d6eb4f594a91ba18d61c5bc1d314Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2ef70e822941461a8426e5277efdae27Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-2ef70e822941461a8426e5277efdae27PubChem References
These sources are listed in the compound's public database record.
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