HCID 20328344, compound → 1-Methyl-4-(10-bromo-5H-dibenzo[a,d]cyclohepten5-ylidene)-piperidine

HRID 917841Notes

Reaction equation

HRID 917841 reaction equation
CC(C)([O-])C.[K+].Br.[CH3:8][N:9]1[CH2:14][CH2:13][C:12](=[C:15]2[C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=3[CH:19]([Br:26])[CH:18](Br)[C:17]3[CH:28]=[CH:29][CH:30]=[CH:31][C:16]2=3)[CH2:11][CH2:10]1>C(O)(C)(C)C>[CH3:8][N:9]1[CH2:14][CH2:13][C:12](=[C:15]2[C:16]3[CH:31]=[CH:30][CH:29]=[CH:28][C:17]=3[CH:18]=[C:19]([Br:26])[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]2=3)[CH2:11][CH2:10]1

Participants

4

Reactant 2

HCID 20328344HCID 20328344, compoundHCID 23665647Potassium tert-butoxide

Product 1

HCID 123688821-Methyl-4-(10-bromo-5H-dibenzo[a,d]cyclohepten5-ylidene)-piperidine

Reagents, catalysts & solvents 1

HCID 6386tert-ButanolSolvent

Procedure

To 600 ml. of a 0.40 M (0.24 mole) solution of potassium t-butoxide in t-butanol is added 42.1 g. (0.079 mole) of 1-methyl-4-(10,11-dibromo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine hydrobromide and the mixture stirred vigorously under anhydrous conditions for 6 hours at room temperature. The reaction mixture is poured into 2 L. of water and extracted 3 times with 100 ml. each of benzene. The combined benzene extracts are dried over anhydrous MgSO4, filtered, the MgSO4 washed with benzene, and the benzene solution evaporated to dryness on a rotary evaporator. There remains 27.9 g. of crystalline product. This product is recrystallized by dissolving in 750 ml. of boiling hexane, filtered hot, the volume reduced to 200 ml. by boiling off hexane, seeding and allowing to crystallize. The crystals are collected and dried in a vacuum oven at 60° overnight to give 1-methyl-4-(10-bromo-5H-dibenzo[a,d]cyclohepten-5-ylidene)piperidine, m.p. 127°-129°C. Three more recrystallizations from hexane gives an analytical sample with m.p. 130°-131° C.

Workup

  1. additionThe reaction mixture is poured into 2 L
  2. extractionof water and extracted 3 times with 100 ml
  3. dry with materialThe combined benzene extracts are dried over anhydrous MgSO4
  4. filtrationfiltered
  5. washthe MgSO4 washed with benzene
  6. customthe benzene solution evaporated to dryness on a rotary evaporator
  7. customThis product is recrystallized
  8. dissolutionby dissolving in 750 ml
  9. filtrationof boiling hexane, filtered hot
  10. customto crystallize
  11. customThe crystals are collected
  12. customdried in a vacuum oven at 60° overnight

Sources & evidence

ORD record
ord-87024c480ebf4ef3844f22a3a1b2bb1d
Source dataset
uspto-grants-1976_07
Patent number
US03968115

Reaction notes

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