(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

HRID 1887392노트

반응식

HRID 1887392 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

6

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

  1. temperaturewas heated
  2. temperatureat reflux under an atmosphere of argon for 3 hours
  3. temperaturethen heating
  4. temperatureat reflux
  5. extractionthe product extracted into diethyl ether (2×30 mL)
  6. washThe combined organic layers were washed with brine (25 mL)
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered

출처 및 근거

ORD 기록
ord-83399376f7214be481204cf2bd7a6324
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08501744B2

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