戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 370313作成日:2026年10月25日

Morpholine → 4-Hydroxy-4,5-dimethyl-2-trimethylsilanyl-dihydrothiophene-3-carboxylic acid allylamide

https://huagongshe.com/reaction/370313

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物3-Mercapto-2-butanoneHCID 38679—
反応物N-allyl-3-trimethylsilylpropiolic amideHCID 11217610—
溶媒DiethoxymethaneHCID 10024—
生成物4-Hydroxy-4,5-dimethyl-2-trimethylsilanyl-dihydrothiophene-3-carboxylic acid allylamideHCID 7014544684%

反応手順

A solution of 3-mercapto-2-butanone (2.1 g, 0.020 mol) and morpholine (1.5 g, 0.017 mol) in diethoxymethane (20 mL) was heated to reflux and treated with N-allyl-3-trimethylsilylpropiolic amide (3.04 g, 0.017 mol). The mixture is heated at reflux under a nitrogen atmosphere overnight. An additional portion of the 3-mercapto-2-butanone (0.7 g, 0.0067 mol) was added, and heating was continued for 4 hours more. A final portion of the 3-mercapto-2-butanone (0.7 g, 0.0067 mol) was added, heating was continued for 4 hours at reflux, then the mixture was cooled and evaporated under reduced pressure. The residue was extracted with two 40 mL portions of hot heptane, filtered, and allowed to cool (ice/salt bath). The resulting solid precipitate was collected by filtration and dried to give 4.0 g of 4-hydroxy-4,5-dimethyl-2-trimethylsilanyl-dihydrothiophene-3-carboxylic acid allylamide (84% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06140511
出典データセットuspto-grants-2000_10
ORD IDord-da4fd3de976e4fca9523abb5cfbba84b
出典メモuspto-grants-2000_10