3-Butenoic acid, ion(1-) → (3R,5S) t-butyl 6-acetoxy-3,5-dihydroxyhexanoate
반응식
[OH:1][C@H:2]([CH2:11][C@H:12]([OH:15])[CH2:13][OH:14])[CH2:3][C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5].C([CH2:18][C:19]([O-])=[O:20])=C>O1CCCC1>[C:19]([O:14][CH2:13][C@@H:12]([OH:15])[CH2:11][C@@H:2]([OH:1])[CH2:3][C:4]([O:6][C:7]([CH3:10])([CH3:8])[CH3:9])=[O:5])(=[O:20])[CH3:18]참가 물질
4
실험 절차
To a stirred 11 round bottom flask 700 ml tetrahydrofuran and 70.7 g (0.32 mol) of (3R,5S) t-butyl 3,5,6-trihydroxyhexanoate, 41 ml (0.46 mol) vinylacetate and 6.3 g of the supported lipase Chirazyme L2′ were charged. After 3 hours stirring at ambient temperature the lipase was removed by screening and the volatiles removed by distillation under vacuum. The mass of crude oil was 78.7 g and the major component was determined to be (3R,5S) t-butyl 6-acetoxy-3,5-dihydroxyhexanoate. This material was used directly in the next stage.
후처리
- addition′ were charged
- customwas removed by screening
- customthe volatiles removed by distillation under vacuum
출처 및 근거
- ORD 기록
- ord-f2bfecf93598413ebb4cf2155f2a2ec6
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732171B2
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