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HRID 1082158作成日:2026年10月27日

Triethylamine → 2-Formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester

https://huagongshe.com/reaction/1082158

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2-Formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid allyl esterHCID 53735263—
溶媒DimethylformamideHCID 6228—
生成物2-Formyl-3-(tert-butyldimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl esterHCID 5381227993.8%

反応手順

To a solution of 15 g of 2-formyl-3-hydroxy -5-methoxy-6-methylbenzoic acid allyl ester in 0.12 l of N,N-dimethylformamide were added 13.8 g of tert-butyl-dimethylchlorosilane and 12.0 g of triethylamine. The mixture was stirred for 3 h at room temperature and then evaporated in vacuo. The residue was taken up in 0.4 l of ethyl acetate and the solution was washed successively with 1N hydrochloric acid, water and brine. The organic layer was dried over sodium sulfate. The solvent was evaporated in vacuo and the solid residue was recrystallized from hexane to give 20.5 g of 2-formyl-3-(tert-butyl-dimethylsilanyloxy)-5-methoxy-6-methylbenzoic acid allyl ester as white crystals of m.p. 94°-95° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05589473
出典データセットuspto-grants-1996_12
ORD IDord-3f38b76d913f4cea9dcc0fe7b75e509f
出典メモuspto-grants-1996_12