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HRID 234207作成日:2026年10月26日

Triethylamine → 2-Formyl-5-methoxy-6-methyl-3-[dimethyl-(1,1,2-trimethyl-propyl)silanyloxy]-benzoic acid allyl ester

https://huagongshe.com/reaction/234207

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Dimethylthexylsilyl chlorideHCID 144239—
反応物2-Formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid allyl esterHCID 53735263—
溶媒DimethylformamideHCID 6228—
生成物2-Formyl-5-methoxy-6-methyl-3-[dimethyl-(1,1,2-trimethyl-propyl)silanyloxy]-benzoic acid allyl esterHCID 5371105292.4%

反応手順

To a solution of 75.1 g of 2-formyl-3-hydroxy-5-methoxy-6-methylbenzoic acid allyl ester in 0.6 l of N,N-dimethylformamide were added 81.0 g of dimethyl-(1,1,2-trimethyl-propyl)-chlorosilane and 45.5 g of triethylamine. The mixture was stirred for 4 h at room temperature and then evaporated in vacuo. The residue was taken up in 2 l of ethyl acetate, and the mixture was successively washed with 1N hydrochloric acid and with brine, and dried over sodium sulfate. The solvent was evaporated in vacuo and the residue was crystallized from hexane to give 108.8 g of 2-formyl-5-methoxy-6-methyl-3-[dimethyl-(1,1,2-trimethyl-propyl)silanyloxy]-benzoic acid allyl ester as white crystals of m.p. 81°-82° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594135
出典データセットuspto-grants-1997_01
ORD IDord-bbb2725d2abe4f02a057cbb2e7ae8b3c
出典メモuspto-grants-1997_01