Benzoyl chloride, 3-nitro- → HCID 86654256, compound

HRID 2360384Notes

Reaction equation

HRID 2360384 reaction equation
[I:1][C:2]1[CH:8]=[C:7]([C:9]([F:21])([C:14]([F:20])([F:19])[C:15]([F:18])([F:17])[F:16])[C:10]([F:13])([F:12])[F:11])[CH:6]=[C:5]([I:22])[C:3]=1[NH2:4].[N+:23]([C:26]1[CH:27]=[C:28]([CH:32]=[CH:33][CH:34]=1)[C:29](Cl)=[O:30])([O-:25])=[O:24]>>[I:1][C:2]1[CH:8]=[C:7]([C:9]([F:21])([C:14]([F:19])([F:20])[C:15]([F:16])([F:17])[F:18])[C:10]([F:11])([F:12])[F:13])[CH:6]=[C:5]([I:22])[C:3]=1[NH:4][C:29](=[O:30])[C:28]1[CH:32]=[CH:33][CH:34]=[C:26]([N+:23]([O-:25])=[O:24])[CH:27]=1

Participants

3

Reactant 2

HCID 8495Benzoyl chloride, 3-nitro-HCID 58297563HCID 58297563, compound

Product 1

HCID 86654256HCID 86654256, compound

Procedure

According to the method of 4-3 of Example 4, a target compound was prepared from 2,6-diiodo-4-(perfluorobutan-2-yl)aniline and 3-nitrobenzoyl chloride.

Sources & evidence

ORD record
ord-785154e8054f4d49815422246297708e
Source dataset
uspto-grants-2014_04
Patent number
US08686044B2

Reaction notes

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