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4-Hydroxyxylidine → 1-[4-acetyl-1-(4-hydroxy-2,3-dimethyl-phenyl)-2,5-dimethyl-1H-pyrrol-3-yl]-ethanone

HRID 2375405
노트
인쇄 미리보기

반응식

HRID 2375405 반응식
[C:1]([CH:4]([C:12](=O)[CH3:13])[CH:5]([C:9](=[O:11])[CH3:10])[C:6](=O)[CH3:7])(=[O:3])[CH3:2].[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([CH3:23])[C:17]=1[CH3:24]>>[C:9]([C:5]1[C:4]([C:1](=[O:3])[CH3:2])=[C:12]([CH3:13])[N:15]([C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([CH3:23])[C:17]=2[CH3:24])[C:6]=1[CH3:7])(=[O:11])[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 765424-HydroxyxylidineHCID 787303,4-Diacetyl-2,5-hexanedione

생성물 1

HCID 692752881-[4-acetyl-1-(4-hydroxy-2,3-dimethyl-phenyl)-2,5-dimethyl-1H-pyrrol-3-yl]-ethanone

실험 절차

Utilizing the general procedure outlined in Example 48, 1,1,2,2-tetraacetylethane (300 mg, 1.5 mol) and 4-amino-2.3-xylenol (206 mg, 1.5 mmol) reacted to give 1-[4-acetyl-1-(4-hydroxy-2,3-dimethyl-phenyl)-2,5-dimethyl-1H-pyrrol-3-yl]-ethanone as yellow solid: MS (ESI) 300 (M+H)+.

후처리

  1. customreacted

출처 및 근거

ORD 기록
ord-8cf72aeb103043469de7829dfe57a48e
출처 데이터셋
uspto-grants-2008_12
DOI
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
10.6084/m9.figshare.5104873.v1
특허 번호
US07465730B2

반응 노트

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