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Sodium hydride → HCID 86607686、化合物

HRID 1295088
ノート
印刷プレビュー

反応式

HRID 1295088 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24758Sodium hydrideHCID 69061805HCID 69061805、化合物

生成物 1

HCID 86607686HCID 86607686、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-c7e763e7c9814d9a9b402312eff92c42
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07241792B2

反応ノート

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