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HRID 59677作成日:2026年10月24日

tert-Butyldimethylsilyl chloride → Methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoate

https://huagongshe.com/ja/reaction/59677

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物DiisopropylethylamineHCID 81531—
反応物Methyl 2-hydroxy-6-methylbenzoateHCID 584223—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoateHCID 8970514770.5%

反応手順

A mixture of methyl 2-hydroxy-6-methylbenzoate (prepared according to Doehner et al, WO 01/05739, 10.0 g), tert-butyldimethylsilyl chloride (11.0 g), N,N-di-isopropylethylamine (32 mL) and DMAP (0.75 g) in DCM (400 mL) was stirred at room temperature overnight. The mixture was washed with water and brine, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and pentane with a gradient of 0-10% to give methyl 2-(tert-butyldimethylsilyloxy)-6-methylbenzoate (11.9 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440943B2
出典データセットuspto-grants-2016_09
ORD IDord-1ffebf94257d437d9795d4aab41dedd1
出典メモuspto-grants-2016_09