Butanal → 1,1-Di-(5 nitroindol-3-yl)-butane

HRID 6941

Reaction equation

HRID 6941 reaction equation

[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH:8]=[CH:7]2)([O-:3])=[O:2].[CH:13](=O)[CH2:14][CH2:15][CH3:16]>>[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH:8]=[C:7]2[CH:13]([C:7]1[C:6]2[C:10](=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[NH:9][CH:8]=1)[CH2:14][CH2:15][CH3:16])([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 261Butanal

HCID 225235-Nitroindole

Product 1

HCID 220192851,1-Di-(5 nitroindol-3-yl)-butane

Procedure

ST 1429 was prepared from 5-nitroindole and butyraldehyde prepared using the method described in example 2/1.

Workup

customprepared

Sources & evidence

ORD record: ord-f5f5a80157ad4bdca616f4b651e2eecb
Source dataset: uspto-grants-2006_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07084166B2

Linked notes

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