Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Potassium Carbonate → (2,3-Dihydro-1,4-benzoxathiin-2-yl)acetonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Phenol, o-mercapto-(6CI,7CI,8CI) | HCID 70718 | — |
| 반응물 | 3,4-Dibromobutanenitrile | HCID 11831139 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | (2,3-Dihydro-1,4-benzoxathiin-2-yl)acetonitrile | HCID 20540157 | — |
반응 단계
The starting material is prepared as follows: To the stirred, refluxing solution of 21 g of 2-hydroxy-thiophenol in 290 ml of acetone is added dropwise 12.5 g of 3,4-dibromo-butyronitrile along with small portions of 15.8 g of anhydrous potassium carbonate. After 30 minutes, the double addition procedure with said amounts of dibromo compound and potassium carbonate is repeated, and after a further 30 minutes said procedure is repeated a third time. The mixture is then refluxed for 20 hours, cooled, filtered, the residual salts washed with acetone, and the filtrate evaporated. The residue is distilled (bulb to bulb), and the fraction boiling at 185°/0.5 mm Hg collected, to yield the 2-(1,4-benzoxathian-2-yl)-acetonitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04129655 |
| 출처 데이터셋 | uspto-grants-1978_12 |
| ORD ID | ord-3cf8bb51fd534efaaea82d7a6cc71de6 |
| 출처 메모 | uspto-grants-1978_12 |