Fumaronitrile → HCID 178444283, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][CH:10]=[CH:11][C@H:12]2[CH2:17][CH2:16][C@H:15]([CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[CH2:14][CH2:13]2)=[CH:4][CH:3]=1.[C:23](#[N:28])/[CH:24]=[CH:25]/[C:26]#[N:27]>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[CH:10][C:11]([C@H:12]3[CH2:13][CH2:14][C@H:15]([CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[CH2:16][CH2:17]3)=[C:25]([C:26]#[N:27])[C:24]=2[C:23]#[N:28])=[CH:4][CH:3]=1Participants
3
Procedure
Using 1-(p-fluorophenyl)-4-(trans-4'-n-pentylcyclohexyl)-1,3-butadiene and fumaronitrile, 3-(p-fluorophenyl)-6-(trans-4'-n-pentylcyclohexyl)phthalonitrile was obtained by the same method as in Example 1. m.p. was 102.5° C.
Sources & evidence
- ORD record
- ord-25e223b0c0d6461d99537dcd58bd0ad1
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04479885
Reaction notes
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