Hydrogen Bromide → (4-Fluorophenyl)(4-phenyl-4-piperidinyl)methanone hydrobromide hemihydrate

HRID 371098Notes

Reaction equation

HRID 371098 reaction equation
[F:1][C:2]1[CH:26]=[CH:25][C:5]([C:6]([C:8]2([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:13][CH2:12][N:11](C(OCC)=O)[CH2:10][CH2:9]2)=[O:7])=[CH:4][CH:3]=1.[BrH:27]>O>[OH2:7].[BrH:27].[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([C:8]2([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[O:7])=[CH:25][CH:26]=1.[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([C:8]2([C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[O:7])=[CH:25][CH:26]=1.[BrH:27]

Participants

4

Procedure

A mixture of 14 parts of ethyl 4-(4-fluorobenzoyl)-4-phenyl-1-piperidinecarboxylate and 150 parts of a hydrobromic acid solution 48% in water was stirred and refluxed for 30 minutes. The reaction mixture was diluted with 100 parts of water and the whole was stirred while the mixture was allowed to cool to room temperature. The precipitated product was filtered off (filtrate I was set aside), washed with methylbenzene and stirred in 2-propanone. It was filtered off again (filtrate II was set aside) and dried, yielding a first fraction of 4.3 parts of (4-fluorophenyl) (4-phenyl-4-piperidinyl)methanone hydrobromide hemihydrate.

Workup

  1. temperaturerefluxed for 30 minutes
  2. stirringthe whole was stirred while the mixture
  3. filtrationThe precipitated product was filtered off (filtrate I
  4. washwashed with methylbenzene
  5. stirringstirred in 2-propanone
  6. filtrationIt was filtered off again (filtrate II
  7. customdried

Sources & evidence

ORD record
ord-541bbf7e06ae422bb632af75b6902500
Source dataset
uspto-grants-1985_07
Patent number
US04529727

Reaction notes

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