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

HRID 1512554
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HRID 1512554 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-94eefd45ccdb420d836a1638f1c257e4
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08217066B2

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