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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843361Generated: October 31, 2026

Ammonia → 4-(Trifluoromethyl)benzylamine

https://huagongshe.com/reaction/843361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBenzaldehyde, 4-(trifluoromethyl)-, oximeHCID 3056297—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
Product4-(Trifluoromethyl)benzylamineHCID 7680492.6%

Reaction Steps

The second step of the process of the present invention was conducted as follows. At first, a 1-liter autoclave equipped with a mechanical stirrer was charged with 300 g (1.59 mol) of 4-trifluoromethylbenzaldehyde oxime, 460 g of 2-propanol, and 15 g of a catalyst (i.e., a carbon powder (50% wet) carrying thereon 5% palladium), followed by introduction of 40 g of liquid ammonia and then introduction of hydrogen to have a pressure of 1 MPa. Then, the reaction mixture was stirred, while the reaction temperature was maintained at 20° C. and while hydrogen was gradually introduced into the autoclave in a manner to maintain the total pressure at 1 MPa. After conducting the reaction for 4 hr, the reaction was stopped, followed by removing the catalyst by filtration. As a result of analyzing the obtained reaction liquid by gas chromatography, 4-trifluoromethylbenzylamine was formed at a yield of 92.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376712B2
Source datasetuspto-grants-2002_04
ORD IDord-ce719a45096c4cd0aa5b7e5dcbf82557
Source noteuspto-grants-2002_04