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Sodium borohydride → [3-(2-Hydroxymethyl-4-methyl-phenoxy)-phenyl]-acetic acid ethyl ester

HRID 885239
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인쇄 미리보기

반응식

HRID 885239 반응식
[CH2:1]([O:3][C:4](=[O:22])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][C:14]=2[CH:20]=[O:21])[CH:7]=1)[CH3:2].[BH4-].[Na+]>CO>[CH2:1]([O:3][C:4](=[O:22])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][C:14]=2[CH2:20][OH:21])[CH:7]=1)[CH3:2]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 58237466[3-(2-Formyl-4-methyl-phenoxy)-phenyl]-acetic acid ethyl ester

생성물 1

HCID 58237434[3-(2-Hydroxymethyl-4-methyl-phenoxy)-phenyl]-acetic acid ethyl ester수율 99.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To [3-(2-formyl-4-methyl-phenoxy)-phenyl]-acetic acid ethyl ester (0.20 g, 0.67 mmol) in MeOH (20 mL) was added sodium borohydride (0.03 g, 0.8 mmol), and the reaction was stirred for 10 minutes at room temperature. Once no starting material was seen by analytical tlc, the mixture was worked-up to give the desired product (0.20 g).

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출처 및 근거

ORD 기록
ord-adc23719ba724b6197ff409fc72a1b39
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242145B2

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