(3aS,6S,6aS)-6-(tert-butyldimethylsilyloxy)tetrahydrofuro[3,2-b]furan-3(2H)-one → tert-butyldimethyl((3R,3aS,6aR)-6-methylene hexahydrofuro[3,2-b]furan-3-yloxy)silane
반응식
[CH3:1]C(C)([O-])C.[K+].[Si:7]([O:14][C@@H:15]1[C@H:19]2[O:20][CH2:21][C:22](=O)[C@H:18]2[O:17][CH2:16]1)([C:10]([CH3:13])([CH3:12])[CH3:11])([CH3:9])[CH3:8]>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O1CCCC1.O>[C:10]([Si:7]([CH3:8])([CH3:9])[O:14][C@@H:15]1[CH2:16][O:17][C@@H:18]2[C:22](=[CH2:1])[CH2:21][O:20][C@H:19]12)([CH3:11])([CH3:12])[CH3:13]참가 물질
반응물 2
생성물 1
시약·촉매·용매 3
실험 절차
A stirred suspension of methyltriphenylphosphonium bromide (1.84 g, 5.16 mmol) and potassium tert-butoxide (578 mg, 5.16 mmol) in tetrahydrofuran (15 mL) was heated at reflux under an atmosphere of argon for 3 hours then allowed to cool to ambient temperature. A solution of ketone (87) (888 mg, 3.44 mmol) in tetrahydrofuran (7.5 mL) was added then heating at reflux continued for 2.25 hours. The mixture was diluted with water (30 mL) then the product extracted into diethyl ether (2×30 mL). The combined organic layers were washed with brine (25 mL), dried (MgSO4), filtered and reduced in vacuo to leave residue (2.07 g). Flash chromatography over silica, eluting with ethyl acetate:heptane mixtures 0:100 to 15:85 gave alkene (88) as a colourless oil (799 mg, 91%).
후처리
- temperaturewas heated
- temperatureat reflux under an atmosphere of argon for 3 hours
- temperaturethen heating
- temperatureat reflux
- extractionthe product extracted into diethyl ether (2×30 mL)
- washThe combined organic layers were washed with brine (25 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
출처 및 근거
- ORD 기록
- ord-83399376f7214be481204cf2bd7a6324
- 출처 데이터셋
- uspto-grants-2013_08
- 특허 번호
- US08501744B2
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