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Sodium hydride → 2-Chloromethyl-2-(2-fluoro-4-trifluoromethylphenyl)oxirane

HRID 1732151
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HRID 1732151 반응식
[Cl:1][CH2:2][C:3]([C:7]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:8]=1[F:17])([OH:6])[CH2:4]Cl.[H-].[Na+]>C(O)(C)(C)C>[Cl:1][CH2:2][C:3]1([C:7]2[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:8]=2[F:17])[CH2:4][O:6]1
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참가 물질

4

반응물 2

HCID 24758Sodium hydrideHCID 202266801,3-Dichloro-2-(2-fluoro-4-trifluoromethylphenyl)-2-propanol

생성물 1

HCID 202267062-Chloromethyl-2-(2-fluoro-4-trifluoromethylphenyl)oxirane

시약·촉매·용매 1

HCID 6386tert-Butanol용매

반응 조건

온도
100 °C

실험 절차

1,3-Dichloro-2-(2-fluoro-4-trifluoromethylphenyl)-2-propanol (7 g.) was added to a solution of sodium hydride (1.45 g. of 48% dispersion in oil) in tert-butyl alcohol (30 ml.) and heated at 100° C. for 1 hour. The mixture was evaporated to dryness and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and dried with anhydrous magnesium sulphate, and the filtered solution was evaporated to dryness to give 2-chloromethyl-2-(2-fluoro-4-trifluoromethylphenyl)oxirane as a yellow oil.

후처리

  1. customThe mixture was evaporated to dryness
  2. customthe residue was partitioned between ethyl acetate and water
  3. customThe organic layer was separated
  4. washwashed with water
  5. dry with materialdried with anhydrous magnesium sulphate
  6. customthe filtered solution was evaporated to dryness

출처 및 근거

ORD 기록
ord-14125b150e614f768159db7134bf899e
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04625036

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