反应 #4148185
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-5fcd5e17d439484ab2f67d02c8dd4469暂无可渲染的结构数据
CC(C)(C)SC1=CC=C(C=C1)N产品信息
4-(tert-butylsulfanyl)aniline(CAS 16463-18-6)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。
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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5fcd5e17d439484ab2f67d02c8dd4469反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5fcd5e17d439484ab2f67d02c8dd4469反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 4-(t-butylmercapto)nitrobenzene (52.8 g., 0.25 mol) and iron powder (150 g.) in 1 l. of water there was added 1 ml. of acetic acid. The reaction mixture was stirred 18 hours at 90° C. and filtered. Both the residue and filtrate were extracted several times with methylene dichloride, and the combined dried methylene dichloride extracts were concentrated at reduced pressure to give 18.2 g. of a brown oil. This is a 40% weight yield of 4-(t-butylmercapto)aniline. To this oil in 100 ml. of benzene there was then added dropwise 158 g. of a 12.5% benzene solution of phosgene (0.2 mol) with cooling. The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature and then at reflux temperature for 7 hours. After standing overnight the reaction mixture was filtered, the filtrate concentrated at reduced pressure, then vacuum-distilled. Two product fractions were collected as filtered Both the residue and filtrate were extracted several times with methylene dichloride were concentrated at reduced pressure to give 18.2 g The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature at reflux temperature for 7 hours After standing overnight the reaction mixture was filtered the filtrate concentrated at reduced pressure vacuum-distilled Two product fractions were collected as
来源 ID: ord-cf72c76e56fb436d9add06f9f7dfe9d2反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 4-(t-butylmercapto)nitrobenzene (52.8 g., 0.25 mol) and iron powder (150 g.) in 1 l. of water there was added 1 ml. of acetic acid. The reaction mixture was stirred 18 hours at 90° C. and filtered. Both the residue and filtrate were extracted several times with methylene dichloride, and the combined dried methylene dichloride extracts were concentrated at reduced pressure to give 18.2 g. of a brown oil. This is a 40% weight yield of 4-(t-butylmercapto)aniline. To this oil in 100 ml. of benzene there was then added dropwise 158 g. of a 12.5% benzene solution of phosgene (0.2 mol) with cooling. The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature and then at reflux temperature for 7 hours. After standing overnight the reaction mixture was filtered, the filtrate concentrated at reduced pressure, then vacuum-distilled. Two product fractions were collected as filtered Both the residue and filtrate were extracted several times with methylene dichloride were concentrated at reduced pressure to give 18.2 g The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature at reflux temperature for 7 hours After standing overnight the reaction mixture was filtered the filtrate concentrated at reduced pressure vacuum-distilled Two product fractions were collected as
来源 ID: ord-cf72c76e56fb436d9add06f9f7dfe9d2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a cold (dry ice - acetone bath) stirred solution of 4-tert-butylthioaniline (25.6 g., 0.14 mole) in methylene chloride is added a slurry of N-bromosuccinimide (25.0 g., 0.14 mole) in methylene chloride in three equal portions. The reaction is allowed to come to room temperature with stirring overnight. The methylene chloride solution is washed with dilute aqueous sodium carbonate and water and then evaporated to give the desired product as a brown oil. to come to room temperature The methylene chloride solution is washed with dilute aqueous sodium carbonate and water evaporated
来源 ID: ord-dcc08a60178d45f3a0ea7038e57a7b88反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 4-(t-butylmercapto)nitrobenzene (52.8 g., 0.25 mol) and iron powder (150 g.) in 1 l. of water there was added 1 ml. of acetic acid. The reaction mixture was stirred 18 hours at 90° C. and filtered. Both the residue and filtrate were extracted several times with methylene dichloride, and the combined dried methylene dichloride extracts were concentrated at reduced pressure to give 18.2 g. of a brown oil. This is a 40% weight yield of 4-(t-butylmercapto)aniline. To this oil in 100 ml. of benzene there was then added dropwise 158 g. of a 12.5% benzene solution of phosgene (0.2 mol) with cooling. The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature and then at reflux temperature for 7 hours. After standing overnight the reaction mixture was filtered, the filtrate concentrated at reduced pressure, then vacuum-distilled. Two product fractions were collected as filtered Both the residue and filtrate were extracted several times with methylene dichloride were concentrated at reduced pressure to give 18.2 g The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature at reflux temperature for 7 hours After standing overnight the reaction mixture was filtered the filtrate concentrated at reduced pressure vacuum-distilled Two product fractions were collected as
来源 ID: ord-ae82541e0eda4f689ff0cef497b9811a反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 4-(t-butylmercapto)nitrobenzene (52.8 g., 0.25 mol) and iron powder (150 g.) in 1 l. of water there was added 1 ml. of acetic acid. The reaction mixture was stirred 18 hours at 90°C. and filtered. Both the residue and filtrate were extracted several times with methylene dichloride, and the combined dried methylene dichloride extracts were concentrated at reduced pressure to give 18.2 g. of a brown oil. This is a 40% weight yield of 4-(t-butylmercapto)aniline. To this oil in 100 ml. of benzene there was then added dropwise 158 g. of a 12.5% benzene solution of phosgene (0.2 mol) with cooling. The reaction mixture was stirred for 1 hour at 10°C., overnight at room temperature and then at reflux temperature for 7 hours. After standing overnight the reaction mixture was filtered, the filtrate concentrated at reduced pressure, then vacuum-distilled. Two product fractions were collected as filtered Both the residue and filtrate were extracted several times with methylene dichloride were concentrated at reduced pressure to give 18.2 g The reaction mixture was stirred for 1 hour at 10°C., overnight at room temperature at reflux temperature for 7 hours After standing overnight the reaction mixture was filtered the filtrate concentrated at reduced pressure vacuum-distilled Two product fractions were collected as
来源 ID: ord-184cde98b9c3465cac1e559225e8ebef反应条件: temp:90.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 4-(t-butylmercapto)nitrobenzene (52.8 g., 0.25 mol) and iron powder (150 g.) in 1 l. of water there was added 1 ml. of acetic acid. The reaction mixture was stirred 18 hours at 90° C. and filtered. Both the residue and filtrate were extracted several times with methylene dichloride, and the combined dried methylene dichloride extracts were concentrated at reduced pressure to give 18.2 g. of a brown oil. This is a 40% weight yield of 4-(t-butylmercapto)aniline. To this oil in 100 ml. of benzene there was then added dropwise 158 g. of a 12.5% benzene solution of phosgene (0.2 mol) with cooling. The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature and then at reflux temperature for 7 hours. After standing overnight the reaction mixture was filtered, the filtrate concentrated at reduced pressure, then vacuum-distilled. Two product fractions were collected as filtered Both the residue and filtrate were extracted several times with methylene dichloride were concentrated at reduced pressure to give 18.2 g The reaction mixture was stirred for 1 hour at 10° C., overnight at room temperature at reflux temperature for 7 hours After standing overnight the reaction mixture was filtered the filtrate concentrated at reduced pressure vacuum-distilled Two product fractions were collected as
来源 ID: ord-cf72c76e56fb436d9add06f9f7dfe9d2PubChem References
以下资料来自该化合物的公开数据库参考记录。
