4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-carbonitrile → 5-(1-Cyano-4-oxa-cyclohexyl)-2-methoxybenzaldehyde
Reaction equation
[C:1]([C:3]1([C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1)#[N:2].C(C1(C2C=CC(OC)=C(C=2)[CH:27]=[O:28])CC1)#N>>[C:1]([C:3]1([C:9]2[CH:10]=[CH:11][C:12]([O:15][CH3:16])=[C:13]([CH:14]=2)[CH:27]=[O:28])[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1)#[N:2]Participants
3
Procedure
This compound was prepared from Compound 88 in the same manner of Compound 2.
Sources & evidence
- ORD record
- ord-f6c66ea9c77649a7b9f653c0566a6187
- Source dataset
- uspto-grants-1998_08
- Patent number
- US05789423
Reaction notes
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