Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → 2H-Pyran, tetrahydro-2-(2-iodoethoxy)-
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Iodoethanol | HCID 17859945 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 2H-Pyran, tetrahydro-2-(2-iodoethoxy)- | HCID 11118662 | — |
반응 단계
Freshly distilled dihydropyran (Aldrich, 59.0 g, 0.7 mol) was added dropwise to a cooled solution of iodoethanol (Aldrich, 98 g, 0.57 mol) in Et2O (1 L) containing 0.1 g of p-toluenesulfonic acid (Eastman). The solution was then stirred for 1 h at 5°. Solid K2CO3 (Mallinckrodt, 5 g) was then added to the reaction mixture and the resulting suspension stirred an additional 1 h at RT. The reaction was then filtered and the remaining solid washed with Et2O (1 L). The organic solutions were combined and concentrated on a rotary evaporator (in a flask washed with 1% NEt3 in H2O). The crude 2-(2-iodoethoxy)tetrahydro-2-H-pyran (100 g, 68.9%) was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04808625 |
| 출처 데이터셋 | uspto-grants-1989_02 |
| ORD ID | ord-7aa641c3f1c844ac85b5ba92271b12c8 |
| 출처 메모 | uspto-grants-1989_02 |