Hydrochloric Acid → HCID 178467954, compound
Reaction equation
[F:1][C:2]1[CH:17]=[CH:16][C:5]([C:6](/[C:8](=[C:11](/N(C)C)\[CH3:12])/[C:9]#[N:10])=[O:7])=[CH:4][CH:3]=1.Cl.C[OH:20]>>[F:1][C:2]1[CH:17]=[CH:16][C:5]([C:6](/[C:8](=[C:11](/[OH:20])\[CH3:12])/[C:9]#[N:10])=[O:7])=[CH:4][CH:3]=1Participants
4
Procedure
A solution of 1.35 g. (0.006 m) of 2-(p-fluorobenzoyl)-3-dimethylaminocrotononitrile in a mixture of 15 ml. methanol and 8 ml. of 1 N HCl was heated on the steam bath in an open beaker for 45 minutes. Upon cooling in an ice bath, a solid formed, was collected, and then recrystallized from cyclohexane-petroleum ether with charcoal treatment, giving 0.7 g. (64%) of light pinkish crystals, m.p. 65°-67° C.
Workup
- temperatureUpon cooling in an ice bath
- customa solid formed
- customwas collected
- customrecrystallized from cyclohexane-petroleum ether with charcoal treatment
- customgiving 0.7 g
Sources & evidence
- ORD record
- ord-b0ab40d4d4ac4b22833e7e55655796b5
- Source dataset
- uspto-grants-1979_11
- Patent number
- US04173650
Reaction notes
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