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HRID 132101作成日:2026年10月25日

Tetrahydrofuran → 1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid

https://huagongshe.com/reaction/132101

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl esterHCID 59733770—
生成物1-(3-Tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acidHCID 59733731107.2%

反応手順

A 1.0 M solution of tetrabutylammonium fluoride in tetrahydrofuran (15.0 mL, 15.0 mmol) was added to 1-(3-tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid 2-trimethylsilanyl-ethyl ester (2.67 mg, 7.16 mmol). After stirring for 16 h, the solution was concentrated, diluted with 10% aqueous hydrochloric acid, and extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated to yield 2.09 g (100% yield) of 1-(3-tert-butyl-phenyl)-3-methylene-cyclohexanecarboxylic acid as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07385085B2
出典データセットuspto-grants-2008_06
ORD IDord-89e0d65b0b0a4531a37e2452c69aba3f
出典メモuspto-grants-2008_06