戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 4507作成日:2026年10月24日

tert-Butanol → 1-[3-(1,1-Dimethylethoxy)-2-hydroxypropyl]pyrrolidine

https://huagongshe.com/ja/reaction/4507

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物EpichlorohydrinHCID 7835—
反応物Sodium HydroxideHCID 14798—
反応物PyrrolidineHCID 31268—
触媒Tin tetrachlorideHCID 24287—
溶媒WaterHCID 962—
生成物1-[3-(1,1-Dimethylethoxy)-2-hydroxypropyl]pyrrolidineHCID 1409709082.6%

反応条件

温度50 °C

反応手順

A mixture of 100.0 g (1.35 m) of tert.butyl alcohol and 51.4 g (1.35 m) of epichlorohydrin in 240 ml of xylenes was stirred and heated to 50° C. Tin (IV) chloride (3.5 g; 1.6 ml; 0.031 m) was added all at once and the reaction mixture immediately exothermed to about 100° C. The reaction mixture was stirred at about 50° C. for 1.5 hrs then cooled to 5° C. while a mixture of 97 g of 50% sodium hydroxide solution and 195 g of ice was added followed by 115.1 g (1.62 m) of pyrrolidine. The reaction mixture was stirred and heated to reflux for 1 hr. The reaction mixture was cooled to RT, diluted with 1 liter of water and extracted with ether. The ether soluble portion was dried and concentrated in vacuo to give 92.4 g of oil which was distilled at 97.5°-97° C./0.075 mm to yield 63.85 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727072
出典データセットuspto-grants-1988_02
ORD IDord-a628bb901d9b42bc84a06439d0456eed
出典メモuspto-grants-1988_02