Hydrochloric Acid → 2',4',6'-Triiodo-3',5'-bis(ethyl)-3-nitrobiphenyl-4-carboxylic acid

HRID 1976511

반응식

HRID 1976511 반응식
[I:1][C:2]1[C:7]([CH2:8][CH3:9])=[C:6]([I:10])[C:5]([C:11](=O)[CH3:12])=[C:4]([I:14])[C:3]=1[C:15]1[CH:20]=[CH:19][C:18]([C:21]([OH:23])=[O:22])=[C:17]([N+:24]([O-:26])=[O:25])[CH:16]=1.Cl>>[I:1][C:2]1[C:7]([CH2:8][CH3:9])=[C:6]([I:10])[C:5]([CH2:11][CH3:12])=[C:4]([I:14])[C:3]=1[C:15]1[CH:20]=[CH:19][C:18]([C:21]([OH:23])=[O:22])=[C:17]([N+:24]([O-:26])=[O:25])[CH:16]=1

참가 물질

3

실험 절차

Freidel-Crafts acylation is performed on 2′,4′,6′-triiodo-3′-ethyl-3-nitrobiphenyl-4-carboxylic acid (13) in the presence of AlCl3 and CH3COCl to yield 2′,4′,6′-triiodo-3′-ethyl-5′-acetyl-3-nitrobiphenyl-4-carboxylic acid (17). 2′,4′,6′-triiodo-3′-ethyl-5′-acetyl-3-nitrobiphenyl-4-carboxylic acid (17) is then reacted with a zinc mercury amalgam and hydrochloric acid and heated to yield 2′,4′,6′-triiodo-3′,5′-bis(ethyl)-3-nitrobiphenyl-4-carboxylic acid (18)

후처리

  1. temperatureheated

출처 및 근거

ORD 기록
ord-92d09aa078ed4cfaa75f40464c50a149
출처 데이터셋
uspto-grants-2001_05
특허 번호
US06226352B1

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