戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 619321作成日:2026年10月24日

Carbon Dioxide → 3-Adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoic acid

https://huagongshe.com/ja/reaction/619321

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Hydrochloric AcidHCID 313—
反応物Ammonium ChlorideHCID 25517—
反応物3-(1-Adamantyl)-4-(t-butyldimethylsilyloxy)bromobenzeneHCID 10788316—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物3-Adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoic acidHCID 13633559—

反応条件

温度-78 °C

反応手順

9.3 g of (2-adamantan-1-yl-4-bromo-phenoxy)-tert-butyl-dimethylsilane were dissolved in 120 ml of absolute tetrahydro-furan and treated dropwise at -78° C. with 15.5 ml of a 1.6 molar solution of n-butyl-lithium in hexane. After stirring at -78° C. for 1.5 hours, a vigorous stream of carbon dioxide was introduced for one hour. Subsequently, the reaction mixture was firstly poured into ice-cold, saturated, aqueous ammonium chloride solution, acidified cautiously to pH 3 with cold 2N hydrochloric acid and extracted with ethyl acetate. After washing once with water, drying over sodium sulfate and evaporation there was obtained a white, crystalline mass which was recrystallized from ethyl acetate and gave 7 g of 3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoic acid. m.p. 250-252° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05958956
出典データセットuspto-grants-1999_09
ORD IDord-368773ed1f4c461dbc131217641165c6
出典メモuspto-grants-1999_09