反应 #4168350
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1747d6eb4f594a91ba18d61c5bc1d314暂无可渲染的结构数据
CC1=C(C(=CC=C1)Cl)N产品信息
2-氯-6-甲基苯胺(CAS 87-63-8)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1747d6eb4f594a91ba18d61c5bc1d314反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2ef70e822941461a8426e5277efdae27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-05377de3043546988f4ae1f5ce95abd7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-92ce3c7961ed413187ebfa5af0096141反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ea10b5eb72704d1c898486b5ed1d556e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ee7954c1f5064386ace3158d762215f4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c869de14804c46189f65d8dd38181291反应条件: temp:7.51; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-0b895c720cf94b4c9cbfbee5dd2e3a55反应条件: temp:7.51; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-c8ae5b2e49c64cb1bd87c65406178cfa反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1747d6eb4f594a91ba18d61c5bc1d314反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2ef70e822941461a8426e5277efdae27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2ef70e822941461a8426e5277efdae27PubChem References
以下资料来自该化合物的公开数据库参考记录。
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