3-Phenoxybenzyl alcohol → 3-Phenoxybenzyl 2-(4-chlorophenylamino)-3-methylbutanimidate

HRID 126980

Reaction equation

HRID 126980 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH:9]([CH:14]([CH3:16])[CH3:15])[C:10](=[NH:13])[O:11][CH3:12])=[CH:4][CH:3]=1.[O:17]([C:24]1[CH:25]=[C:26]([CH:29]=[CH:30][CH:31]=1)CO)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][CH:9]([CH:14]([CH3:16])[CH3:15])[C:10](=[NH:13])[O:11][CH2:12][C:26]2[CH:29]=[CH:30][CH:31]=[C:24]([O:17][C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:25]=2)=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 262953-Phenoxybenzyl alcoholHCID 12767220Methyl 2-(4-chlorophenylamino)-3-methylbutanimidate

Product 1

HCID 127672213-Phenoxybenzyl 2-(4-chlorophenylamino)-3-methylbutanimidate

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

A solution of 2.25 g (10 mmol) of methyl 2-(4-chlorophenylamino)-3-methylbutanimidate and 4.00 g (20 mmol) of 3-phenoxybenzyl alcohol is heated with continuous removal of methanol. Upon cessation of methanol evolution, there is obtained an oil, 3-phenoxybenzyl 2-(4-chlorophenylamino)-3-methylbutanimidate.

Sources & evidence

ORD record
ord-25c9c6c8c5294111bda856bf486330e4
Source dataset
uspto-grants-1981_03
Patent number
US04254264

Linked notes

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