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HCID 54016540, 화합물 → HCID 18416718, 화합물

HRID 565310
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HRID 565310 반응식
C([O:3][C:4](=[O:26])[C:5]([S:15]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)(=[O:17])=[O:16])([CH3:14])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([Br:13])=[CH:9][CH:8]=1)C>CO.[OH-].[Na+]>[Br:13][C:10]1[CH:9]=[CH:8][C:7]([CH2:6][C:5]([S:15]([C:18]2[CH:19]=[CH:20][C:21]([O:24][CH3:25])=[CH:22][CH:23]=2)(=[O:17])=[O:16])([CH3:14])[C:4]([OH:26])=[O:3])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 54016540HCID 54016540, 화합물

생성물 1

HCID 18416718HCID 18416718, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 14798Sodium Hydroxide용매

실험 절차

3-(4-Bromo-phenyl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-propionic acid was prepared starting from 3-(4-bromo-phenyl)-2-(4-methoxy-benzenesulfonyl)-2-methyl-propionic acid ethyl ester (4.0 g, 9.0 mmol) dissolved in methanol (50 ml) and 10 N NaOH (30 ml). The resulting reaction mixture was worked up as outlined in Example 9. Yield 3.0 g, 78%. Low melting solid. MS: 413 (M+H)+.

후처리

  1. customThe resulting reaction mixture

출처 및 근거

ORD 기록
ord-58923415ca7942ba88a0f3e3e8ba2dec
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06172057B2

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