Epichlorohydrin → 4-(2-Oxiranylmethoxy)benzenecarbonitrile
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1)#[N:2].[CH2:10]([CH:12]1[O:14][CH2:13]1)Cl>>[O:14]1[CH2:13][CH:12]1[CH2:10][O:9][C:6]1[CH:7]=[CH:8][C:3]([C:1]#[N:2])=[CH:4][CH:5]=1Participants
3
Procedure
The sub-title compound was prepared in 75% yield according to the procedure described International Patent Application WO 99/31100 (i.e. by reaction between p-cyanophenol and epichlorohydrin).
Sources & evidence
- ORD record
- ord-8c7af5cd0a2746a69e209d5bf4ce360c
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07144914B2
Reaction notes
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