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HRID 23783作成日:2026年10月26日

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol

https://huagongshe.com/reaction/23783

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物Sodium BicarbonateHCID 516892—
反応物(S)-3-(t-butyldimethylsilyloxy)-5-(4-methoxy-benzyloxy)-1-phenyl pentaneHCID 69589755—
溶媒Water methylene chlorideHCID 21908982—
生成物(S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-olHCID 6958999399.4%

反応手順

(S)-3-(t-butyl dimethylsilyloxy)-5-(4-methoxy-benzyloxy)-1-phenyl pentane (15 g, 36.2 mmol) was dissolved in a solvent mixture of dichloromethane-water (20:1) (252 ml). DDQ (8.2 g, 36.2 mmol) was added thereto and the mixture was stirred for 30 minutes at room temperature. After completion of the reaction, saturated aqueous NaHCO3 solution (100 ml) was added to the reaction solution to stop the reaction. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The organic layers were combined, washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to give (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol (10.6 g, Yield 99%) of a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852880B2
出典データセットuspto-grants-2005_02
ORD IDord-1c47ced5a42f41fc94e54e9b138b5b44
出典メモuspto-grants-2005_02