Potassium tert-butoxide → tert-butyldimethyl((3R,3aS,6aR)-6-methylene hexahydrofuro[3,2-b]furan-3-yloxy)silane

HRID 2168175노트

반응식

HRID 2168175 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-2846e54726a94f90886273653e67f231
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09045492B2

반응 노트

불러오는 중…