반응식
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10]O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Br-:12].[Br-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CO>C(#N)C>[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][Br:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1참가 물질
5
실험 절차
To a solution of 4-phenyl-1-butanol (21.75 g) in acetonitrile (300 mL) was added triphenylphosphine dibromide (67.23 g) in portions with stirring over 10 min. After stirring over night under nitrogen, methanol (4 mL) was added and after 1.5 h, the solvent was removed under reduced pressure. Hexanes (200 mL) and ˜75 g silica gel were added to the residue and the mixture was filtered and the filter cake was eluted with hexanes. The clear filtrate was concentrated to give 32.8 g of clear colorless liquid. This product was again eluted through silica gel using 1.5 L hexanes to give the title compound (24.7 g) as a colorless liquid.
후처리
- stirringAfter stirring over night under nitrogen
- customthe solvent was removed under reduced pressure
- additionHexanes (200 mL) and ˜75 g silica gel were added to the residue
- filtrationthe mixture was filtered
- washthe filter cake was eluted with hexanes
- concentrationThe clear filtrate was concentrated
출처 및 근거
- ORD 기록
- ord-06693a3616814cb881bb4b289a4578b1
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06358979B1
연결된 노트
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