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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658085Generated: October 25, 2026

3-(Bromomethyl)-5-(trifluoromethyl)benzonitrile → 3-(Aminomethyl)-5-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/658085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)-5-(trifluoromethyl)benzonitrileHCID 11601369—
ReactantAmmonia methanolHCID 21705897—
Product3-(Aminomethyl)-5-(trifluoromethyl)benzonitrileHCID 45115840—

Reaction Conditions

Temperature55 °C

Reaction Steps

3-Bromomethyl-5-trifluoromethyl-benzonitrile (which is prepared in Reference Example 12) (15.9 g) is dissolved in 7M-ammonia/methanol (550 ml), and the mixture is stirred at 50-60° C. for 30 minutes. The reaction solution is concentrated under reduced pressure. To the resulting residue are added a saturated aqueous sodium bicarbonate solution and chloroform, and the mixture is separated, and the organic layer is dried over sodium sulfate, and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (chloroform:methanol=1:0→19:1→chloroform:methanol:ammonium hydroxide solution=19:1:0.1) to give 3-aminomethyl-5-trifluorometyl-benzonitrile (10.4 g). MS (m/z): 201 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076364B2
Source datasetuspto-grants-2011_12
ORD IDord-59a4312b22d24405804e93c91807a522
Source noteuspto-grants-2011_12