반응 #6660

ord-3d2de9dc77a241a391535aaa38779401

반응 방정식

COc1cccc([C@]2(O)CCCC[C@H]2CN(C)C)c1
(−)-tramadol
[H-].[K+]
potassium hydride
Sc1ccccc1
thiophenol
CN(C)C[C@H]1CCCC[C@]1(O)c1cccc(O)c1
O-desmethyl tramadol

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도being maintained at <50° C
  2. 2
    기타The final reaction mixture
  3. 3
    온도was heated slowly
  4. 4
    온도to reflux for 45 minutes
  5. 5
    온도The mixture was cooled
  6. 6
    기타quenched into water
  7. 7
    추출the mixture was extracted with ethyl ether
  8. 8
    추출the resulting mixture was extracted 5 more times with methylene chloride
  9. 9
    기타The extract was dried
  10. 10
    기타the 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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE039221E1uspto-grants-2006_08