反应 #4118399
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-95d65ee1d50a470d8bf3fa481e6173ae暂无可渲染的结构数据
CC(C)(CC(=O)OC)N产品信息
3-氨基-3-甲基丁酸甲酯(CAS 29637-56-7)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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11 条反应 · 11 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-95d65ee1d50a470d8bf3fa481e6173ae反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3d05cfda189342238d7ebf5a5b2a6883反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3-amino-3-methyl-butyric acid 10-1 (1 eq.) in methanol at 0° C. was added 2 eq. of thionyl chloride. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was evaporated to give azeotropic mixture of 10-2 and toluene (x=3) which was used for Step B. MS: MH+=132.1 The solvent was evaporated to give azeotropic
来源 ID: ord-12eab62409644f549ff42be168d97b7a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3-amino-3-methyl-butyric acid 10-1 (1 eq.) in methanol at 0° C. was added 2 eq. of thionyl chloride. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was evaporated to give azeotropic mixture of 10-2 and toluene (x=3) which was used for Step B. MS: MH+=132.1 The solvent was evaporated to give azeotropic
来源 ID: ord-bb6106fff1594252865d9d33fdecda9a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3-amino-3-methyl-butyric acid 10-1 (1 eq.) in methanol at 0° C. was added 2 eq. of thionyl chloride. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was evaporated to give azeotropic mixture of 10-2 and toluene (x=3) which was used for Step B. MS: MH+=132.1 The solvent was evaporated to give azeotropic
来源 ID: ord-bb6106fff1594252865d9d33fdecda9a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-95d65ee1d50a470d8bf3fa481e6173ae反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3d05cfda189342238d7ebf5a5b2a6883反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3-amino-3-methyl-butyric acid 10-1 (1 eq.) in methanol at 0° C. was added 2 eq. of thionyl chloride. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was evaporated to give azeotropic mixture of 10-2 and toluene (x=3) which was used for Step B. The solvent was evaporated to give azeotropic
来源 ID: ord-9ff4ab00f3534463aec2dd6e09a36aad反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3-amino-3-methyl-butyric acid 10-1 (1 eq.) in methanol at 0° C. was added 2 eq. of thionyl chloride. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was evaporated to give azeotropic mixture of 10-2 and toluene (x=3) which was used for Step B. MS: MH+=132.1 The solvent was evaporated to give azeotropic
来源 ID: ord-12eab62409644f549ff42be168d97b7a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 3-amino-3-methyl-butyric acid 10-1 (1 eq.) in methanol at 0° C. was added 2 eq. of thionyl chloride. The reaction mixture was warmed to room temperature and stirred overnight. The solvent was evaporated to give azeotropic mixture of 10-2 and toluene (x=3) which was used for Step B. MS: MH+=132.1 The solvent was evaporated to give azeotropic
来源 ID: ord-bb6106fff1594252865d9d33fdecda9a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3d05cfda189342238d7ebf5a5b2a6883PubChem References
以下资料来自该化合物的公开数据库参考记录。
