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Lithium borohydride → [5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-methanol

HRID 1183266
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HRID 1183266 반응식
C[O:2][C:3]([C:5]1[C:6]([CH3:17])=[N:7][O:8][C:9]=1[C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][CH:11]=1)=O.[BH4-].[Li+]>CCO>[Br:16][C:13]1[CH:12]=[CH:11][C:10]([C:9]2[O:8][N:7]=[C:6]([CH3:17])[C:5]=2[CH2:3][OH:2])=[CH:15][CH:14]=1
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참가 물질

4

반응물 2

HCID 4148881Lithium borohydrideHCID 56604575Methyl 5-(4-bromophenyl)-3-methylisoxazole-4-carboxylate

생성물 1

HCID 58218538[5-(4-Bromo-phenyl)-3-methyl-isoxazol-4-yl]-methanol

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
60 °C

실험 절차

5-(4-Bromo-phenyl)-3-methyl-isoxazole-4-carboxylic acid methyl ester (5 g, 16.8 mmol) and lithium borohydride (1.85 g, 84.1 mmol) were combined in EtOH and stirred at 60° C. After aqueous workup, the crude material was purified by silica gel chromatography to give the title compound.

후처리

  1. customAfter aqueous workup, the crude material was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-f1f87bf6c65f4fedbc6ff09c4e4ae778
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08664220B2

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