反应 #1178485

ord-cc9905dbfa404b7187cd27cc1a476058

反应方程式

C[C@@H]1COC[C@H](C)N1C(=O)OC(C)(C)C
Cis-4-tert-butoxycarbonyl-3,5-dimethylmorpholine
C1COCCO1.Cl
hydrochloric acid 1,4-dioxane
C[C@@H]1COC[C@H](C)N1.Cl
title compound
C[C@@H]1COC[C@H](C)N1.Cl
Cis-3,5-dimethylmorpholine hydrochloride

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The reaction liquor was concentrated under reduced pressure
  2. 2
    其他dried

实验过程

Cis-4-tert-butoxycarbonyl-3,5-dimethylmorpholine g, 8.18 mmol) was dissolved in 4N-hydrochloric acid/1,4-dioxane (50 mL), and the solution was stirred for 3 days at room temperature. The reaction liquor was concentrated under reduced pressure and dried, to obtain the title compound as an oily matter. This compound was used in the subsequent reaction without performing further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08129366B2uspto-grants-2012_03