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Potassium Hydroxide → [(2S)-7-(Trifluoromethylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methanol

HRID 39013
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인쇄 미리보기

반응식

HRID 39013 반응식
C([O:4][C:5]1[CH:10]=[C:9]([S:11]([C:14]([F:17])([F:16])[F:15])(=[O:13])=[O:12])[CH:8]=[CH:7][C:6]=1[O:18][CH2:19][C@H:20]1[CH2:22][O:21]1)(=O)C.[OH-].[K+]>O1CCOCC1>[F:16][C:14]([F:15])([F:17])[S:11]([C:9]1[CH:8]=[CH:7][C:6]2[O:18][CH2:19][C@H:20]([CH2:22][OH:21])[O:4][C:5]=2[CH:10]=1)(=[O:12])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 866529492-[(2R)-Oxiran-2-ylmethoxy]-5-[(trifluoromethyl)sulfonyl]phenyl acetate

생성물 1

HCID 67198869[(2S)-7-(Trifluoromethylsulfonyl)-2,3-dihydro-1,4-benzodioxin-2-YL]methanol

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Preparation according to Preparation 20 using 2-[(2R)-oxiran-2-ylmethoxy]-5-[(trifluoromethyl)sulfonyl]phenyl acetate (1.0 g, 3.7 mmol), dioxane (10 ml) and KOH (10%, 10 ml), the mixture stirred at RT for 1 h. Yield 1.0 g. MS m/z (rel. intensity, 70 eV) 298 (M+, 29), 229 (72), 165 (bp), 107 (67), 79 (33).

후처리

  1. customPreparation

출처 및 근거

ORD 기록
ord-1acb426b52e149b98ebdc866b3fc5ae3
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524766B2

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