Diethyl Ether → 3,3-Diphenylpropene

HRID 78914

반응식

HRID 78914 반응식
[CH2:1]([Li])CCC.[C:6]1([CH:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:13]=O)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.C(OCC)C>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[C:6]1([CH:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:13]=[CH2:1])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

참가 물질

6

반응 조건

온도
0 °C

실험 절차

Methyltriphenylphosphonium bromide (4 g, 11.12 mmol) was added over a 15-min period to a mixture of butyllithium (7.3 ml of 1.6 M solution in THF, 11.76 mmol) and dry THF (50 ml) with stirring and under nitrogen atmosphere at 0° C. The reaction mixture was stirred for 2 h at room temperature and the mixture was then recooled to −78° C. A solution of diphenylacetaldehyde (2.2 g, 11.12 mmol) in dry THF (10 ml) was added to the above mixture over a 15-min period. The reaction mixture was stirred for 24 h at room temperature, followed by addition of ethyl ether (200 ml), and the reaction mixture was then filtered. The ether extracts were washed with water (3×50 ml), brine (100 ml) and dried over anhydrous sodium sulfate. The crude material was purified by flash chromatography on silical gel (Hexane:Ethyl ether=9:1) to give pure 3,3-diphenylpropene 460 mg (46%).

후처리

  1. stirringThe reaction mixture was stirred for 2 h at room temperature
  2. customwas then recooled to −78° C
  3. stirringThe reaction mixture was stirred for 24 h at room temperature
  4. filtrationthe reaction mixture was then filtered
  5. washThe ether extracts were washed with water (3×50 ml), brine (100 ml)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe crude material was purified by flash chromatography on silical gel (Hexane:Ethyl ether=9:1)

출처 및 근거

ORD 기록
ord-4bf15defb2f34096b8dea783c069a5b5
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08841464B2

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