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HRID 77324作成日:2026年10月24日

Triethylamine → 2-(Tert-butyldimethylsilanyloxy)-1-phenylethanone

https://huagongshe.com/ja/reaction/77324

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物alpha-HydroxyacetophenoneHCID 68490—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物2-(Tert-butyldimethylsilanyloxy)-1-phenylethanoneHCID 1352333870.7%

反応手順

To a well stirred solution of 2-hydroxyacetophenone (1.0 g, 7.34 mmol) in dichloromethane (15 mL) is added triethylamine (1.23 mL, 8.81 mmol), 4-dimethylaminopyridine (45 mg, 0.367 mmol) and tert-butyldimethylsilyl chloride (1.16 g, 7.71 mmol) dissolved in dichloromethane (2 mL). The reaction mixture is stirred at room temperature for 1 h, then diluted with dichloromethane (50 mL), washed with 10% citric acid, saturate sodium carbonate, brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is purified via silica gel chromatography (20% ethyl acetate in hexanes) to yield the title compound as a yellow oil (1.3 g, 5.19 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841291B2
出典データセットuspto-grants-2014_09
ORD IDord-bc682cb8ff3148aa8529b9d5ab9e350a
出典メモuspto-grants-2014_09