Triethylamine → (-)-cis-3-Acetoxy-cyclopentanol
반응식
[C:1]([O:4][C@@H:5]1[CH2:9][C@H:8]([OH:10])[CH:7]=[CH:6]1)(=[O:3])[CH3:2].C(N(CC)CC)C>C(O)C.[Ni]>[C:1]([O:4][C@@H:5]1[CH2:6][CH2:7][C@H:8]([OH:10])[CH2:9]1)(=[O:3])[CH3:2]참가 물질
5
실험 절차
Dissolve (-)-cis-4-acetoxy-cyclopent-2-enol (11.0 g, 77.4 mmol, prepared in example 19) in ethanol (50 mL) and treat with Raney nickel (1.1 g, previously washed with water (2×50 mL) and ethanol (2×50 mL), Ra--Ni). Charge the atmosphere with hydrogen at 50 psi (344.74 kPa) and shake the mixture. After 20 minutes, filter the solution and treat the filtrate with triethylamine (1.0 mL, 7.2 mmol). After one hour concentrate the solution under vacuum and distill the residue by Kugelrohr distillation (60°-80° C., 1 mm Hg), to provide the title compound (9.74 g, 87%) as a colorless oil.
후처리
- washpreviously washed with water (2×50 mL) and ethanol (2×50 mL), Ra
- additionCharge the atmosphere with hydrogen at 50 psi (344.74 kPa) and shake the mixture
- filtrationfilter the solution
- concentrationAfter one hour concentrate the solution under vacuum
- distillationdistill the residue
- distillationby Kugelrohr distillation (60°-80° C., 1 mm Hg)
출처 및 근거
- ORD 기록
- ord-f043af33bf7d4a64ba8d85518371337b
- 출처 데이터셋
- uspto-grants-1998_03
- 특허 번호
- US05728899
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