alpha-Methyl-o-(2-phenylethoxy)benzylamine hydrochloride → HCID 178463290, compound

HRID 973178Notes

Reaction equation

HRID 973178 reaction equation
[ClH:1].[CH3:2][CH:3]([NH2:19])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[O:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.Cl.CC(N=[C:38]1[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][NH:39]1)C1C=CC(CCC2C=CC=CC=2)=CC=1>>[ClH:1].[CH3:2][CH:3]([N:19]=[C:38]1[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][NH:39]1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[O:10][CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

3

Reactant 2

HCID 13012114alpha-Methyl-o-(2-phenylethoxy)benzylamine hydrochlorideHCID 178463294HCID 178463294, compound

Product 1

HCID 178463290HCID 178463290, compound

Procedure

Substituting this amine for the α-methyl-ρ-phenethylbenzylamine of Example IV results in the formation of hexahydro-2-[α-methyl-o-(2-phenylethoxy)benzylimino]azepine hydrochloride, having a M.P. of 189°-90° C. (dec.)

Sources & evidence

ORD record
ord-ce4b85b4c3204ced8cbd8e794ed660bb
Source dataset
uspto-grants-1977_10
Patent number
US04055561

Reaction notes

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