反应 #444658

ord-751273514a5d4d02b8be4f0496d72038

反应方程式

CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O
ampicillin
Cl
HCl
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O.O.O.O
title compound
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O.O.O.O
Ampicillin Trihydrate

试剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度while cooling with ice
  2. 2
    其他The aqueous phase is separated off
  3. 3
    萃取the organic phase back-extracted with a mixture of 5.4 ml concentrated HCl and 44.5 ml water
  4. 4
    过滤The combined aqueous phases are filtered through a filtering aid
  5. 5
    workup.ADDITIONpumped into a suspension of 5 g ampicillin trihydrate seed crystals in 100 ml water keeping the pH from 4.5 to 5.0
  6. 6
    workup.ADDITIONby the addition of concentrated aqueous ammonia

实验过程

The resultant crude protected ampicillin mixture is worked up by treating with a mixture of 289 ml ice-water and 39.6 ml concentrated HCl and stirred for 30 minutes while cooling with ice. The aqueous phase is separated off and the organic phase back-extracted with a mixture of 5.4 ml concentrated HCl and 44.5 ml water. The combined aqueous phases are filtered through a filtering aid and pumped into a suspension of 5 g ampicillin trihydrate seed crystals in 100 ml water keeping the pH from 4.5 to 5.0 by the addition of concentrated aqueous ammonia. The title compound is obtained by standing the mixture overnight in a refrigerator, isolating the crystals, and washing them with 60 ml ice-water and 3×50 ml 90% acetone, followed by drying. Yield 61.6 g=82.4%, Purity 98.8%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05840885uspto-grants-1998_11