Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 5-(4-Heptylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Diethyl cyanophosphonate | HCID 76257 | — |
| 반응물 | Benzoic acid, 4-heptyl- | HCID 170036 | — |
| 반응물 | 4,5,6,7-Tetrahydrofuro[3,2-c]pyridine hydrochloride | HCID 19599941 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-(4-Heptylbenzoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridine | HCID 19600004 | — |
반응 단계
To a solution of 0.160 g (1.000 mmol) of 4,5,6,7-tetrahydrofuro[3,2-c]pyridine hydrochloride, 0.264 g (1.2 mmol) of 4-heptylbenzoic acid and 0.55 ml (4.0 mmol) of triethylamine in 30 ml of dichloromethane, 0.24 g (1.5 mmol) of diethyl cyanophosphonate was added under ice-cooling, followed by overnight stirring at room temperature. This solution was poured into water and extracted with dichloromethane 2 times. The combined organic layer was washed with water and dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to yield the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05998433 |
| 출처 데이터셋 | uspto-grants-1999_12 |
| ORD ID | ord-e747f5d9f7f64e0cb2378b73f0dfa507 |
| 출처 메모 | uspto-grants-1999_12 |