Hydrochloric Acid → Hydrocodone

HRID 1293510노트

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HRID 1293510 반응식
CC(C)([O-])C.[K+].C(C1C=CC=CC=1)(=O)C1C=CC=CC=1.[CH3:21][N:22]1[C@@H:38]2[CH2:39][C:27]3[CH:28]=[CH:29][C:30]([O:41][CH3:42])=[C:31]4[O:32][C@H:33]5[C@@H:34]([OH:40])[CH2:35][CH2:36][C@@H:37]2[C@:25]5([C:26]=34)[CH2:24][CH2:23]1.Cl>C1C=CC=CC=1>[CH3:21][N:22]1[C@@H:38]2[CH2:39][C:27]3[CH:28]=[CH:29][C:30]([O:41][CH3:42])=[C:31]4[O:32][C@H:33]5[C:34]([CH2:35][CH2:36][C@@H:37]2[C@:25]5([C:26]=34)[CH2:24][CH2:23]1)=[O:40]

참가 물질

6

실험 절차

To a mixture of 1.25 g (11.1 mmol) of potassium-t-butoxide in 50 mL of benzene were added 6.78 g (37 mmol) of benzophenone and 1.12 g (3.7 mmol) of dihydrocodeine, which was allowed to reflux for 2 hours. The reaction mixture turned yellow. The reaction mixture was allowed to cool to room temperature, and 50 mL of 2N HCl was added. The resulting reaction mixture was allowed to stir for 10 minutes. The organic layer was separated and extracted with 3×40 mL of 2N HCl. The organic layer was discarded, and the aqueous layer was again extracted with 3×20 mL of dichloromethane. The aqueous layer was basified with aqueous potassium hydroxide solution to pH 12 and extracted with 5×60 mL of dichloromethane. The organic layers were combined and dried over MgSO4 and filtered. The filtrate was concentrated to give 691 mg (2.3 mmol, 55%) of 3 as a yellow solid.

후처리

  1. temperatureto reflux for 2 hours
  2. customThe resulting reaction mixture
  3. customThe organic layer was separated
  4. extractionextracted with 3×40 mL of 2N HCl
  5. extractionthe aqueous layer was again extracted with 3×20 mL of dichloromethane
  6. extractionextracted with 5×60 mL of dichloromethane
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-7325940d50b741c28d3a8f18834ff74c
출처 데이터셋
uspto-grants-2007_07
특허 번호
US07238791B1

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