Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 6,6-Difluoro-5-methyl-5-hexenyl methanesulfonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | Methyl 6,6-difluoro-5-methyl-5-hexenol | HCID 23020199 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6,6-Difluoro-5-methyl-5-hexenyl methanesulfonate | HCID 23020371 | 99.6% |
반응 단계
To 100 ml of tetrahydrofuran, 5.00 g (33 mmol) of methyl 6,6-difluoro-5-methyl-5-hexenol and 4.20 g (37 mmol) of methanesulfonyl chloride were dissolved, followed by drop-wisely adding 4.40 g (44 mmol) of triethylamine under ice-cooling. After the end of the drop-wise addition, the reaction liquid was stirred at room temperature for 1 hour. Hydrochloric acid salt of triethylamine was filtered, followed by adding water to the filtrate and extracting with ethyl acetate. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentrating under reduced pressure to obtain 7.50 g (yield: 99%) of 6,6-difluoro-5-methyl-5-hexenyl methanesulfonate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07273878B2 |
| 출처 데이터셋 | uspto-grants-2007_09 |
| ORD ID | ord-002d529bf0d3487ebd5e33d89e7c7885 |
| 출처 메모 | uspto-grants-2007_09 |