Hydrochloric Acid → alpha-(3-Chloropropyl)-2-thiophenemethanol

HRID 352108

반응식

HRID 352108 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)=[O:6].[BH4-].[Na+].Cl>C(O)C>[Cl:1][CH2:2][CH2:3][CH2:4][CH:5]([C:7]1[S:8][CH:9]=[CH:10][CH:11]=1)[OH:6]

참가 물질

5

반응 조건

온도
0 °C

실험 절차

4-Chloro-1-(2-thienyl)-1-butanone (9.37 g, 50 mmol) was dissolved in ethanol (100 ml) and the solution cooled to 0° C. Sodium borohydride (1.88 g, 50 mmol) was added in one portion and the reaction allowed to warm to room temperature, then stirred for 18 hours. Aqueous 2M hydrochloric acid was added dropwise until the reaction ceased to effervesce. The solvent was removed in vacuo and the residue partitioned between water and ethyl acetate. The layers were separated and the aqueous portion extracted with ethyl acetate (2×100 ml). The combined organic portions were washed with water (50 ml), dried (magnesium sulphate), filtered and evaporated. The residue was passed down a flash silica chromatography column, eluting with hexane: ethyl acetate (4:1) to afford the title compound as a pale straw coloured oil (7.58 g, 79%).

후처리

  1. temperatureto warm to room temperature
  2. customThe solvent was removed in vacuo
  3. customthe residue partitioned between water and ethyl acetate
  4. customThe layers were separated
  5. extractionthe aqueous portion extracted with ethyl acetate (2×100 ml)
  6. washThe combined organic portions were washed with water (50 ml)
  7. dry with materialdried (magnesium sulphate)
  8. filtrationfiltered
  9. customevaporated
  10. washeluting with hexane: ethyl acetate (4:1)

출처 및 근거

ORD 기록
ord-0e7b09ba79084a2fa6c77f1fe6042d27
출처 데이터셋
uspto-grants-2004_06
특허 번호
US06743939B2

연결된 노트

불러오는 중…