HCID 10401480, compound → HCID 19776778, compound

HRID 1612835Notes

Reaction equation

HRID 1612835 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[O:9][CH:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1.Cl[CH2:23][CH2:24][CH2:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[N+:33]([O-:35])=[O:34]>>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[O:9][CH:10]1[CH2:11][CH2:12][N:13]([CH2:23][CH2:24][CH2:25][O:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[N+:33]([O-:35])=[O:34])[CH2:14][CH2:15]1

Participants

3

Reactant 2

HCID 10401480HCID 10401480, compoundHCID 114244631-(3-Chloro-propoxy)-2-nitro-benzene2×

Product 1

HCID 19776778HCID 19776778, compound

Procedure

The procedure of Example 24 (a) was repeated except for using 4-[(2-methylphenyl)-phenylmethoxy]piperidine and 1-chloro-3-(2-nitrophenoxy)propane instead of 4-[(2-chlorophenyl)-phenylmethoxy]piperidine and 1-chloro-3-(2-nitrophenoxy)propane to give oily 4-[(2-methylphenyl)-phenylmethoxy]-1-[3-(2-nitrophenoxy)propyl]piperidine.

Sources & evidence

ORD record
ord-e014eb4993744bef9eb2d65ab51984ca
Source dataset
uspto-grants-1993_03
Patent number
US05190959

Reaction notes

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