反应 #3844400
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-8af99ba76541467cb7946fdcf8aef99a暂无可渲染的结构数据
COC(=O)C1CSCN1产品信息
噻唑烷-4-羧酸甲酯(CAS 60667-24-5)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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数据库编号 93329
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合成路线数据
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8af99ba76541467cb7946fdcf8aef99a反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Hydrogen chloride gas was bubbled through a suspension of L-thioproline (990 mg, 7.55 mmol) in MeOH (30 mL) cooled at 0° C. for 5 min. The resulting clear solution was stirred at RT for 2 h, then concentrated carefully under reduced pressure. The obtained residue was dried in vacuo overnight to give a white solid, which was dissolved in MeOH (30 mL) and treated with Diaion® WA21J resin (6 g). The resulting suspension was stirred at RT for 30 min, then filtered. The filtrate was concentrated carefully under reduced pressure and the oily residue stripped with toluene (2×) to give a colorless oil. concentrated carefully under reduced pressure The obtained residue was dried in vacuo overnight to give a white solid, which The resulting suspension was stirred at RT for 30 min filtered The filtrate was concentrated carefully under reduced pressure to give a colorless oil
来源 ID: ord-78af3367829e452ea289a9d47f2137d7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8af99ba76541467cb7946fdcf8aef99a反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Hydrogen chloride gas was bubbled through a suspension of L-thioproline (990 mg, 7.55 mmol) in MeOH (30 mL) cooled at 0° C. for 5 min. The resulting clear solution was stirred at RT for 2 h, then concentrated carefully under reduced pressure. The obtained residue was dried in vacuo overnight to give a white solid, which was dissolved in MeOH (30 mL) and treated with Diaion® WA21J resin (6 g). The resulting suspension was stirred at RT for 30 min, then filtered. The filtrate was concentrated carefully under reduced pressure and the oily residue stripped with toluene (2×) to give a colorless oil. concentrated carefully under reduced pressure The obtained residue was dried in vacuo overnight to give a white solid, which The resulting suspension was stirred at RT for 30 min filtered The filtrate was concentrated carefully under reduced pressure to give a colorless oil
来源 ID: ord-d760ad7fe85b4db28a5027f71961ae09反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2.2 g of methyl thiazolidine-4-carboxylate in 50 ml of ether was added dropwise with stirring at ambient temperature 3.14 g of O-ethyl S-propyl phosphoroisocyanatidothioate. The mixture was allowed to react overnight at ambient temperature and was then concentrated by evaporation under reduced pressure to obtain 5.2 (97 percent of theory) of the title compound as a colorless oil having a refractive index at 25° C. of 1.5312. to react overnight at ambient temperature was then concentrated by evaporation under reduced pressure
来源 ID: ord-127e2becfb8343319dcb09eeeb9d3311反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Hydrogen chloride gas was bubbled through a suspension of L-thioproline (990 mg, 7.55 mmol) in MeOH (30 mL) cooled at 0° C. for 5 min. The resulting clear solution was stirred at RT for 2 h, then concentrated carefully under reduced pressure. The obtained residue was dried in vacuo overnight to give a white solid, which was dissolved in MeOH (30 mL) and treated with Diaion® WA21J resin (6 g). The resulting suspension was stirred at RT for 30 min, then filtered. The filtrate was concentrated carefully under reduced pressure and the oily residue stripped with toluene (2×) to give a colorless oil. concentrated carefully under reduced pressure The obtained residue was dried in vacuo overnight to give a white solid, which The resulting suspension was stirred at RT for 30 min filtered The filtrate was concentrated carefully under reduced pressure to give a colorless oil
来源 ID: ord-78af3367829e452ea289a9d47f2137d7PubChem References
以下资料来自该化合物的公开数据库参考记录。
