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HRID 465872作成日:2026年10月25日

Triethylamine → 3-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]benzene bromide

https://huagongshe.com/reaction/465872

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-BromophenolHCID 11563—
反応物Dimethylthexylsilyl chlorideHCID 144239—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
生成物3-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]benzene bromideHCID 1987540794.8%

反応手順

To a stirred solution of 3-bromophenyl alcohol (5.0 g, 26.7 mmol) and triethylamine (3.25 g, 32.1 mmol) in anhydrous CH2Cl2 (125 mL) at room temperature under argon was added dropwise dimethylthexylsilylchloride (5.26 g, 29.4 mmol). After 1.5 hours, 4-dimethylaminopyridine (0.50 g) was added and the stirring was continued for an additional 3 hours. The reaction mixture was diluted with hexane (200 mL) and the precipitate was filtered off. The filtrate was concentrated, partitioned between hexane (200 mL) and 1N aqueous HCl (3×40 mL), and the organic layer was washed with saturated aqueous NaHCO3 (2×40 mL). The organic layer was dried (MgSO4), filtered and concentrated to yield title bromide (8.01 g, 91%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05153327
出典データセットuspto-grants-1992_10
ORD IDord-2120ce38006b45ea849d9d008495a88d
出典メモuspto-grants-1992_10