Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanol → 4-Morpholin-4-yl-4-oxo-2-(2-trifluoromethyl-benzylsulfonylmethyl)-butyric acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 2-(Trifluoromethyl)phenylmethanethiol | HCID 2761423 | — |
| 반응물 | 2-Methylene4-morpholin-4-yl-4-oxo-butyric acid | HCID 22054022 | — |
| 반응물 | Potassium hydroxy sulfite | HCID 23707502 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-Morpholin-4-yl-4-oxo-2-(2-trifluoromethyl-benzylsulfonylmethyl)-butyric acid | HCID 22053989 | — |
반응 단계
A mixture of 2-methylene-4-morpholin-4-yl-4-oxo-butyric acid (2 g, 10.03 mmol), in DMF (5 mL), 2-trifluoromethylbenzyl mercaptan (1.93 g, 10.03 mmol) and DMAP (122 mg, 1.0 mmol) was stirred at ambient temperature for 16 hours. Methanol (200 mL) and a saturated aqueous solution of Oxone® (20 g, 32.5 mmol) were added with continued stirring for 2 hours. Methanol was removed under vacuum and the aqueous residue was diluted with 200 mL of water. The crystallized product was filtered, washed with water, and dried under vacuum to yield 4-morpholin-4-yl-4-oxo-2-(2-trifluoromethyl-benzylsulfonylmethyl)-butyric acid (0.95 g) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07064123B1 |
| 출처 데이터셋 | uspto-grants-2006_06 |
| ORD ID | ord-d2b151c39d9a41da90bb419d88fb61a9 |
| 출처 메모 | uspto-grants-2006_06 |