Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370313생성일: 2026년 10월 25일
Morpholine → 4-Hydroxy-4,5-dimethyl-2-trimethylsilanyl-dihydrothiophene-3-carboxylic acid allylamide
https://huagongshe.com/reaction/370313
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Morpholine | HCID 8083 | — |
| 반응물 | 3-Mercapto-2-butanone | HCID 38679 | — |
| 반응물 | N-allyl-3-trimethylsilylpropiolic amide | HCID 11217610 | — |
| 용매 | Diethoxymethane | HCID 10024 | — |
| 생성물 | 4-Hydroxy-4,5-dimethyl-2-trimethylsilanyl-dihydrothiophene-3-carboxylic acid allylamide | HCID 70145446 | 84% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06140511 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-da4fd3de976e4fca9523abb5cfbba84b |
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| 출처 메모 | uspto-grants-2000_10 |
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