戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1086369作成日:2026年10月27日

Hydrochloric Acid → Tert-butyl 2-methylthio-6-n-hexylcinnamate

https://huagongshe.com/reaction/1086369

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DiisopropylamineHCID 7912—
反応物1,1-Dimethylethyl trimethylsilylacetateHCID 99527—
反応物2-Methylthio-6-n-hexylbenzaldehydeHCID 15008155—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 2-methylthio-6-n-hexylcinnamateHCID 54465638—

反応条件

温度-10 °C

反応手順

To a solution of lithium diisopropylamide, afforded by combining 3.4 g of diisopropylamine with 26 ml of n-butyllithium, at -40° C. in THF is added tert-butyl trimethylsilylacetate (8 g, 0.042 mmol) and the mixture stirred for 1 hour. To the reaction mixture is added 2-methylthio-6-n-hexylbenzaldehyde (7.08 g, 0.03 mmol) dropwise and stirred for 2 hours at -40° C. The reaction mixture is allowed to warm to -10° C. and cold lN HCl poured in. The mixture is extracted with diethyl ether. The extracts are washed with water and then brine, dried over MgSO4 and concentrated to afford tert-butyl 2-methylthio-6-n-hexylcinnamate which is hydrolyzed in methylene chloride with trifluoroacetic acid by refluxing overnight to afford the subtitle compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05028629
出典データセットuspto-grants-1991_07
ORD IDord-819f0ae255ac49a6a097e30ab4ddc585
出典メモuspto-grants-1991_07