Hydrochloric Acid → 5-Methyl-3-Methoxy-5,6,7,8,9,10,11,12-Octahydro-5,11-Methano-Benzocyclodecen-13-One

HRID 2072161Notes

Reaction equation

HRID 2072161 reaction equation
[H-].[Na+].Br[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]Br.[CH3:10][CH:11]1[C:20]2[C:15](=[CH:16][CH:17]=[C:18]([O:21][CH3:22])[CH:19]=2)[CH2:14][CH2:13][C:12]1=[O:23].Cl>C1C=CC=CC=1>[CH3:10][C:11]12[C:12](=[O:23])[CH:13]([CH2:14][C:15]3[CH:16]=[CH:17][C:18]([O:21][CH3:22])=[CH:19][C:20]=31)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]2

Participants

6

Procedure

Oil-free sodium hydride (5.28 g.) in benzene (50 ml.) is added to a stirred mixture of 1,5-dibromopentane (184 g.) and 1-methyl-7-methoxy-2-tetralone (32 g.) in dry benzene (300 ml.). Stirring is continued for 12 hours at 25° and at reflux for an additional 15 hours. The mixture is cooled, sodium hydride (5.8 g.) in 50 ml. benzene added, stirring continued at 25° for 10 hours. and refluxed for 12 additional hours. After cooling excess base is neutralized with concentrated hydrochloric acid and the inorganic solids which precipitate are removed by filtration. Washing and filtrate with saline, drying over sodium sulfate, concentrating and vacuum distilling gives an oil (21 g.), b.p. 160°-190° C. (0.5 mm.) containing 6.5 g. (27%) of the title product by vapor phase chromatography (3% OVI, C200-225-250).

Workup

  1. temperatureat reflux for an additional 15 hours
  2. temperatureThe mixture is cooled
  3. stirringstirring
  4. waitcontinued at 25° for 10 hours
  5. temperatureand refluxed for 12 additional hours
  6. temperatureAfter cooling excess base
  7. customthe inorganic solids which precipitate are removed by filtration
  8. washWashing
  9. dry with materialfiltrate with saline, drying over sodium sulfate
  10. concentrationconcentrating
  11. distillationvacuum distilling
  12. customgives an oil (21 g.), b.p. 160°-190° C. (0.5 mm.)
  13. additioncontaining 6.5 g

Sources & evidence

ORD record
ord-266becd991e0405ca2ee001805b31cc7
Source dataset
uspto-grants-1977_09
Patent number
US04049701

Reaction notes

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