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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943087Generated: November 1, 2026

3-Nitrobenzamide → 3-Aminobenzamide

https://huagongshe.com/reaction/1943087

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzamideHCID 12576—
ReactantHCID 16049389HCID 16049389—
Product3-AminobenzamideHCID 1645—

Reaction Steps

3-nitro-benzoyl chloride was reacted with an aniline, that is 2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenylamine, to form a 3-nitro-benzamide, that is 3-nitro-N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamide, and c) the 3-nitro-benzamide, that is 3-nitro-N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamide, was reduced to afford the desired 3-amino-benzamide, that is 3-amino-N-[2,6-dimethyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamide. Further 3-amino-benzamides were made, for example, by using a substituted 3-nitro-benzoic acid, such as 2-fluoro-3-nitro-benzoic acid, in step a) and/or a different aniline, such as 2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoro-methyl-ethyl)-phenylamine, in step b). Whilst this three step synthesis gives satisfactory results in the laboratory a shorter route to 3-amino-benzamides is required if the carbamate insecticides or bisamide insecticides are to be manufactured on a commercial scale.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389767B2
Source datasetuspto-grants-2013_03
ORD IDord-af8d5e14fc8541f5bc25c27c963cbb9b
Source noteuspto-grants-2013_03