반응 #6660
ord-3d2de9dc77a241a391535aaa38779401
반응 방정식
반응 조건
후처리
- 1온도being maintained at <50° C
- 2기타The final reaction mixture
- 3온도was heated slowly
- 4온도to reflux for 45 minutes
- 5온도The mixture was cooled
- 6기타quenched into water
- 7추출the mixture was extracted with ethyl ether
- 8추출the resulting mixture was extracted 5 more times with methylene chloride
- 9기타The extract was dried
- 10기타the methylene chloride was evaporated
실험 절차
First, O-desmethyl tramadol was prepared as set forth hereinafter. Diethylene glycol (125 mL) was added with cooling to potassium hydride (9.5 g) with the temperature being maintained at <50° C. To the solution was added thiophenol (10 mL) dissolved in diethylene glycol (25 mL), and then (−)-tramadol as the free base (9.3 g) in diethylene glycol (50 mL) was added. The final reaction mixture was heated slowly to reflux for 45 minutes. The mixture was cooled and then quenched into water. The pH was adjusted to about 3, and the mixture was extracted with ethyl ether. The pH was readjusted to about 8 and the resulting mixture was extracted 5 more times with methylene chloride. The extract was dried and the methylene chloride was evaporated to yield 4.6 g of the title compound as an oil. The oil was distilled (Kugelrohr), dissolved in tetrahydrofuran, treated with an ethanol/HCl solution to give 2.3 g of the salt. The salt was recrystallized from ethanol/ethyl ether and dried to yield 1.80 g of the salt of the (−) enantiomer of O-desmethyl tramadol (mp. 242°-3° C.), [α]D25=−32.9 (C=1, EtOH).