Butylamine → 2-(p-Fluorobenzoyl)-3-butylaminocrotononitrile
Reaction equation
[F:1][C:2]1[CH:16]=[CH:15][C:5]([C:6](/[C:8](=[C:11](/OC)\[CH3:12])/[C:9]#[N:10])=[O:7])=[CH:4][CH:3]=1.[CH2:17]([NH2:21])[CH2:18][CH2:19][CH3:20]>>[F:1][C:2]1[CH:16]=[CH:15][C:5]([C:6](/[C:8](=[C:11](/[NH:21][CH2:17][CH2:18][CH2:19][CH3:20])\[CH3:12])/[C:9]#[N:10])=[O:7])=[CH:4][CH:3]=1Participants
3
Procedure
A sample of 2.5 g. of 2-(p-fluorobenzoyl)-3-methoxycrotononitrile is dissolved in 10 ml. of n-butylamine. The solution is sealed in a stainless steel bomb and heated on a steam bath overnight. The bomb is then opened and the solvent evaporated under reduced pressure. A greenish oil is obtained which is distilled on a Kugelrohr apparatus at 200° C./0.1 mm. to obtain the yellow oily product.
Workup
- temperatureheated on a steam bath overnight
- customthe solvent evaporated under reduced pressure
- customA greenish oil is obtained which
- distillationis distilled on a Kugelrohr apparatus at 200° C./0.1 mm
- customto obtain the yellow oily product
Sources & evidence
- ORD record
- ord-b6cb3cc1b5644b3a951ee0f353086208
- Source dataset
- uspto-grants-1979_11
- Patent number
- US04173650
Reaction notes
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