反应 #4034241
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-f31c01ff50c74b1e8517a408911d8d86暂无可渲染的结构数据
C1=CC(=CC(=C1)C(F)(F)F)CS产品信息
3-三氟甲基苄硫醇(CAS 25697-55-6)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 141236
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f31c01ff50c74b1e8517a408911d8d86反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-be3b72c1ea904faa986e56e884b16ad0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5f648fe33f24406b8d99e6a98bc638ca反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b60d5c12c2be4037b7ea2869a904c40a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-763cb844524e484a835bad31866863b9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the stirred suspension of 1.08 g of sodium hydride in 25 ml of dimethylformamide the solution of 9.0 g of m-trifluoromethylbenzylmercaptan in 50 ml of dimethylformamide is added during 3 minutes and the mixture stirred for 10 minutes. It is combined with 7.75 g of 6-methyl-5-nitropyridine-2-carboxylic acid methyl ester and the whole stirred on the steam bath for 30 minutes and allowed to stand overnight at room temperature. 2 ml of acetic acid are added and the solution is mixed with ice water to produce a dense, grainy precipitate. It is filtered off and recrystallized from isopropanol-diethyl ether, to yield the 6-methyl-5-(m-trifluoromethylbenzylmercapto)-pyridine-2-carboxylic acid methyl ester melting at 91°-93°. is added during 3 minutes the whole stirred on the steam bath for 30 minutes to stand overnight at room temperature to produce a dense, grainy precipitate It is filtered off recrystallized from isopropanol-diethyl ether
来源 ID: ord-b557d90e02e242649dbc071b29c93e87反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the stirred suspension of 1.08 g of sodium hydride in 25 ml of dimethylformamide the solution of 9.0 g of m-trifluoromethylbenzylmercaptan in 50 ml of dimethylformamide is added during 3 minutes and the mixture stirred for 10 minutes. It is combined with 7.75 g of 6-methyl-5-nitropyridine-2-carboxylic acid methyl ester and the whole stirred on the steam bath for 30 minutes and allowed to stand overnight at room temperature. 2 ml of acetic acid are added and the solution is mixed with ice water to produce a dense, grainy precipitate. It is filtered off and recrystallized from isopropanol-diethyl ether, to yield the 6-methyl-5-(m-trifluoromethylbenzylmercapto)-pyridine-2-carboxylic acid methyl ester melting at 91°-93°. is added during 3 minutes the whole stirred on the steam bath for 30 minutes to stand overnight at room temperature to produce a dense, grainy precipitate It is filtered off recrystallized from isopropanol-diethyl ether
来源 ID: ord-b557d90e02e242649dbc071b29c93e87反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The solution of 4.6 g of m-trifluoromethylbenzylmercaptan in 30 ml of dimethylformamide is added to the slurry of 1.08 g of 50% sodium hydride in mineral oil (washed 2 times with hexane), under nitrogen while stirring at room temperature. After several minutes, a clear yellow solution is obtained, which is combined with that of 5.0 g of 3-nitro-2,5-pyridinedicarboxylic acid dimethyl ester in 50 ml of dimethylformamide. The mixture is warmed on the steam bath for 30 minutes at 90° and stirred at room temperature overnight. It is acidified with 2 ml of acetic acid and diluted to 400 ml with a mixture of ice and water. The precipitate formed is collected and recrystallized from methanol-diethyl ether (1:1), to yield the 3-(m-trifluoromethylbenzylmercapto)-2,5-pyridine-dicarboxylic acid dimethyl ester melting at 102°-106°. After several minutes a clear yellow solution is obtained The mixture is warmed on the steam bath for 30 minutes at 90° stirred at room temperature overnight The precipitate formed is collected recrystallized from methanol-diethyl ether (1:1)
来源 ID: ord-efd756ed420344f197f24e94481a5b3d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The solution of 4.6 g of m-trifluoromethylbenzylmercaptan in 30 ml of dimethylformamide is added to the slurry of 1.08 g of 50% sodium hydride in mineral oil (washed 2 times with hexane), under nitrogen while stirring at room temperature. After several minutes, a clear yellow solution is obtained, which is combined with that of 5.0 g of 3-nitro-2,5-pyridinedicarboxylic acid dimethyl ester in 50 ml of dimethylformamide. The mixture is warmed on the steam bath for 30 minutes at 90° and stirred at room temperature overnight. It is acidified with 2 ml of acetic acid and diluted to 400 ml with a mixture of ice and water. The precipitate formed is collected and recrystallized from methanol-diethyl ether (1:1), to yield the 3-(m-trifluoromethylbenzylmercapto)-2,5-pyridine-dicarboxylic acid dimethyl ester melting at 102°-106°. After several minutes a clear yellow solution is obtained The mixture is warmed on the steam bath for 30 minutes at 90° stirred at room temperature overnight The precipitate formed is collected recrystallized from methanol-diethyl ether (1:1)
来源 ID: ord-efd756ed420344f197f24e94481a5b3d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the stirred suspension of 1.08 g of sodium hydride in 25 ml of dimethylformamide the solution of 9.0 g of m-trifluoromethylbenzylmercaptan in 50 ml of dimethylformamide is added during 3 minutes and the mixture stirred for 10 minutes. It is combined with 7.75 g of 6-methyl-5-nitropyridine-2-carboxylic acid methyl ester and the whole stirred on the steam bath for 30 minutes and allowed to stand overnight at room temperature. 2 ml of acetic acid are added and the solution is mixed with ice water to produce a dense, grainy precipitate. It is filtered off and recrystallized from isopropanol-diethyl ether, to yield the 6-methyl-5-(m-trifluoromethylbenzylmercapto)-pyridine-2-carboxylic acid methyl ester melting at 91°-93°. is added during 3 minutes the whole stirred on the steam bath for 30 minutes to stand overnight at room temperature to produce a dense, grainy precipitate It is filtered off recrystallized from isopropanol-diethyl ether
来源 ID: ord-d48858b33b3e42dba1cd391f06073333反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the stirred suspension of 1.08 g of sodium hydride in 25 ml of dimethylformamide the solution of 9.0 g of m-trifluoromethylbenzylmercaptan in 50 ml of dimethylformamide is added during 3 minutes and the mixture stirred for 10 minutes. It is combined with 7.75 g of 6-methyl-5-nitropyridine-2-carboxylic acid methyl ester and the whole stirred on the steam bath for 30 minutes and allowed to stand overnight at room temperature. 2 ml of acetic acid are added and the solution is mixed with ice water to produce a dense, grainy precipitate. It is filtered off and recrystallized from isopropanol-diethyl ether, to yield the 6-methyl-5-(m-trifluoromethylbenzylmercapto)-pyridine-2-carboxylic acid methyl ester melting at 91°-93°. is added during 3 minutes the whole stirred on the steam bath for 30 minutes to stand overnight at room temperature to produce a dense, grainy precipitate It is filtered off recrystallized from isopropanol-diethyl ether
来源 ID: ord-b557d90e02e242649dbc071b29c93e87反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f31c01ff50c74b1e8517a408911d8d86PubChem References
以下资料来自该化合物的公开数据库参考记录。
