Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725213Generated: October 29, 2026

Acetic Acid → Benzenemethanamine, N-butyl-2-fluoro-4-(trifluoromethyl)-

https://huagongshe.com/reaction/1725213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantButylamineHCID 8007—
Reactant2-Fluoro-4-(trifluoromethyl)benzaldehydeHCID 522929—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductBenzenemethanamine, N-butyl-2-fluoro-4-(trifluoromethyl)-HCID 6885536926%

Reaction Steps

To a solution of 2-fluoro-4-(trifluoromethyl)benzaldehyde (3.84 g, 20.0 mmol) and n-butylamine (1.46 g, 20.0 mmol) in methanol (100 mL) were added acetic acid (4.6 mL, 80 mmol) and sodium cyanoborohydride (1.51 g, 24.0 mmol) and the solution was stirred at room temperature for 3 days. Water (10 mL) was added and the mixture was concentrated in vacuo. The residue was taken up in aqueous 1 M KOH (125 mL) and ethyl acetate (100 mL) and the phases were separated. The aqueous phase was extracted with ethyl acetate (2×100 mL) and the combined organic phase was dried over Na2SO4 and concentrated in vacuo. Purification on a prepacked column of silica gel (Isolute® SPE Column, 70 g/150 mL) with ethyl acetate (33-100% gradient) in heptane as the eluent and collection of pure fractions yielded 1.28 g (26%) of a colourless oil of low viscosity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488844B2
Source datasetuspto-grants-2009_02
ORD IDord-d4272ae34dbb43f9aafb010a0c0e4fa4
Source noteuspto-grants-2009_02