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Tetrabutylammonium Fluoride → 3-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butan-1-ol

HRID 639827
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인쇄 미리보기

반응식

HRID 639827 반응식
CCCC[N+](CCCC)(CCCC)CCCC.[F-].[Si]([O:26][CH2:27][CH2:28][CH:29]([N:31]1[N:35]=[N:34][C:33]([C:36]2[CH:41]=[CH:40][CH:39]=[C:38]([Cl:42])[CH:37]=2)=[N:32]1)[CH3:30])(C(C)(C)C)(C)C>C1COCC1>[Cl:42][C:38]1[CH:37]=[C:36]([C:33]2[N:34]=[N:35][N:31]([CH:29]([CH3:30])[CH2:28][CH2:27][OH:26])[N:32]=2)[CH:41]=[CH:40][CH:39]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2724141Tetrabutylammonium FluorideHCID 684318752-(3-{[tert-butyl(dimethyl)silyl]oxy}-1-methylpropyl)-5-(3-chlorophenyl)-2H-tetrazole

생성물 1

HCID 684296013-[5-(3-chlorophenyl)-2H-tetrazol-2-yl]butan-1-ol수율 91%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

TBAF was added to a solution of 2-(3-{[tert-butyl(dimethyl)silyl]oxy}-1-methylpropyl)-5-(3-chlorophenyl)-2H-tetrazole in THF (25 mL). The mixture was concentrated after 4 h and the crude was purified by flash column chromatography (SiO2, Heptane-EtOAc 1:1) to give 0.90 g (91%) of the title compound.

후처리

  1. concentrationThe mixture was concentrated after 4 h
  2. customthe crude was purified by flash column chromatography (SiO2, Heptane-EtOAc 1:1)

출처 및 근거

ORD 기록
ord-b3459ad394b14bbaab9ff185ff823a46
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691892B2

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