Dimethylamine → 3-Fluoro-4,5-bis(phenylmethoxy)benzeneacetonitrile
Reaction equation
[CH2:1](C#N)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13](OC)[C:12]=1[OH:19].CN(CC1C=C(F)C(O)=C(OC)C=1)C.[CH2:34]=[O:35].CNC.C(N)[C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1.CI.[C-:49]#[N:50].[Na+].B(Br)(Br)Br.OC1C=C(C=C(F)C=1O)CC#N.C1(C(=CC=CC=1)O)O.[CH2:76](Cl)C1C=CC=CC=1>>[CH2:34]([O:35][C:13]1[CH:14]=[C:15]([CH:16]=[C:11]([F:10])[C:12]=1[O:19][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[CH2:76][C:49]#[N:50])[C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1Participants
Reactant 11
Product 1
Procedure
A process for the preparation of the benzylcyanide compound of the formula I ##STR21## is prepared by: (a) converting the 2-fluoro-6-methoxyphenol compound of the formula II ##STR22## into the N,N-dimethyl-4-hydroxy-3-methoxy-5-fluorobenzylamine compound of the formula III by treating with formaldehyde and N,N-dimethylamine; ##STR23## (b) treating the benzylamine compound of the formula III by treating with methyliodide and displacement with NaCN, into the 3-methoxy-4-hydroxy-5-fluorobenzylnitrile compound of formula IV ##STR24## (c) treating the benzylnitrile compound of the formula IV with BBr3, followed by dibenzylation of the resulting catechol 3,4-dihydroxy-5-fluorobenzylcyanide compound of the formula V ##STR25## with benzylchloride to give the 3,4-dibenzyloxy-5-fluorobenzylcyanide compound of the formula I, ##STR26##
Sources & evidence
- ORD record
- ord-1326d4af251148dab0dee95d78202339
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04855476
Reaction notes
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