反応式
[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]=1参加物
反応条件
- 温度
- 0 °C
実験手順
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%).
後処理
- stirringThe reaction mixture was stirred for 2 h at room temperature
- customwas then recooled to −78° C
- stirringThe reaction mixture was stirred for 24 h at room temperature
- filtrationthe reaction mixture was then filtered
- washThe ether extracts were washed with water (3×50 ml), brine (100 ml)
- dry with materialdried over anhydrous sodium sulfate
- customThe crude material was purified by flash chromatography on silical gel (Hexane:Ethyl ether=9:1)
出典と根拠
- ORDレコード
- ord-4bf15defb2f34096b8dea783c069a5b5
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841464B2
関連ノート
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