Sodium Hydroxide → Ampicillin Sodium

HRID 66053

반응식

HRID 66053 반응식
[CH3:1][C:2]1([CH3:24])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:20])[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:21]([OH:23])=[O:22].O.O.O.[OH-].[Na+:29]>O>[CH3:1][C:2]1([CH3:24])[S:6][C@@H:5]2[C@H:7]([NH:10][C:11]([C@H:13]([NH2:20])[C:14]3[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=3)=[O:12])[C:8](=[O:9])[N:4]2[C@H:3]1[C:21]([O-:23])=[O:22].[Na+:29]

참가 물질

4

반응물 2

HCID 14798Sodium Hydroxide2회HCID 23565Ampicillin Trihydrate

생성물 1

HCID 23663979Ampicillin Sodium

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A suspension of 24.18 gm (60 millimols) of ampicillin trihydrate in 140 ml of water was admixed with 55.2 ml of an aqueous 1N sodium hydroxide solution (8% less than equimolar amount of NaOH) in the manner and under the conditions described in Example 1, and the sodium ampicillin was isolated in exactly the same manner as in Example 1.

출처 및 근거

ORD 기록
ord-177c8f38f14b4e4d99132f91365c0976
출처 데이터셋
uspto-grants-1978_12
특허 번호
US04130558

연결된 노트

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