반응 #444658

ord-751273514a5d4d02b8be4f0496d72038

반응 방정식

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

시약

없음

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도while cooling with ice
  2. 2
    기타The aqueous phase is separated off
  3. 3
    추출the organic phase back-extracted with a mixture of 5.4 ml concentrated HCl and 44.5 ml water
  4. 4
    여과The 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

실험 절차

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%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05840885uspto-grants-1998_11