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Sodium hydride → HCID 86607686, 화합물

HRID 1295088
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HRID 1295088 반응식
[CH:1]1([CH2:4][CH:5]=[CH:6][CH2:7][CH2:8][CH:9]([OH:12])CO)[CH2:3][CH2:2]1.[H-].[Na+]>C1COCC1>[CH:1]1([CH2:4][CH:5]=[CH:6][CH2:7][CH:8]2[CH2:9][O:12]2)[CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 24758Sodium hydrideHCID 69061805HCID 69061805, 화합물

생성물 1

HCID 86607686HCID 86607686, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 7-Cyclopropyl-hept-5-ene-1,2-diol (1.45 g, 9.28 mmol) in THF (30 mL) was added 60% sodium hydride (1.1 g, 27.84 mmol) at 0° C. The mixture was slowly warmed to room temperature and stirred for 1 h. TrisIm (3.41 g, 10.2 mmol) was added in one portion at 0° C. followed stirring at room temperature for 1.5 h. The mixture was quenched with water and extracted with Et2O. The organics were washed with brine, dried over MgSO4, filtered, and concentrated. Purification by silica gel chromatography (7% EtOAc in hexanes gradient to 14% EtOAc in hexanes) gave 2-(4-Cyclopropyl-but-2-enyl)-oxirane as a clear oil; 1H NMR (400 MHz, CDCl3): δ 5.54–5.48 (m, 1H), 5.44–5.37 (m, 1H), 2.94–2.91 (m, 1H), 2.75 (dd, 1H, J1=4.9 Hz, J2=4.1 Hz), 2.48 (dd, 1H, J1=5.0 Hz, J2=2.7 Hz), 2.19 (q, 2H, J=7.3 Hz), 1.98 (t, 2H, J=7.0 Hz), 1.62–1.56 (m, 2H), 0.75–0.66 (m, 1H), 0.44–0.39 (m, 2H), 0.09–0.05(m, 2H).

후처리

  1. additionTrisIm (3.41 g, 10.2 mmol) was added in one portion at 0° C.
  2. stirringfollowed stirring at room temperature for 1.5 h
  3. customThe mixture was quenched with water
  4. extractionextracted with Et2O
  5. washThe organics were washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customPurification by silica gel chromatography (7% EtOAc in hexanes gradient to 14% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-c7e763e7c9814d9a9b402312eff92c42
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241792B2

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