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Lithium hydroxide, monohydrate → 5-[5-(Hydroxymethyl)-1H-tetrazol-1-yl]-2-(trifluoromethyl)benzonitrile

HRID 517726
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HRID 517726 반응식
O.[OH-].[Li+].C([O:7][CH2:8][C:9]1[N:13]([C:14]2[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[C:16]([C:24]#[N:25])[CH:15]=2)[N:12]=[N:11][N:10]=1)(=O)C>C(O)C.O.CCOC(C)=O>[OH:7][CH2:8][C:9]1[N:13]([C:14]2[CH:19]=[CH:18][C:17]([C:20]([F:23])([F:22])[F:21])=[C:16]([CH:15]=2)[C:24]#[N:25])[N:12]=[N:11][N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 86691873{1-[3-Cyano-4-(trifluoromethyl)phenyl]-1H-tetrazol-5-yl}methyl acetate2회

생성물 1

HCID 866918745-[5-(Hydroxymethyl)-1H-tetrazol-1-yl]-2-(trifluoromethyl)benzonitrile수율 27.7%

시약·촉매·용매 3

HCID 702Ethanol용매HCID 962Water용매
HCID 8857
Ethyl Acetate
용매

실험 절차

Lithium hydroxide monohydrate (1.35 g, 32.2 mmol) was added to a solution of {1-[3-cyano-4-(trifluoromethyl)phenyl]-1H-tetrazol-5-yl}methyl acetate (Intermediate 39, 5.0 g, 16.1 mmol) in a mixture of ethanol and water (2:1) at 0° C. The reaction mixture was stirred for 6 h at room temperature. The reaction mixture was diluted with EtOAc and washed with ice-water. The organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford the crude compound. This was purified by column chromatography (100-200 mesh silica gel), eluting with 20%-60% EtOAc/pet.ether to give the title compound (1.2 g).

후처리

  1. washwashed with ice-water
  2. dry with materialThe organic layer was dried over anhydrous Na2SO4
  3. concentrationconcentrated under reduced pressure
  4. customto afford the crude compound
  5. customThis was purified by column chromatography (100-200 mesh silica gel)
  6. washeluting with 20%-60% EtOAc/pet

출처 및 근거

ORD 기록
ord-f131b5b1b96944f4b4dfccd5981d02ee
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115132B2

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