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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480368Generated: October 30, 2026

Trifluoroacetic acid → HCID 39417231, compound

https://huagongshe.com/reaction/480368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 4-FormylbenzoateHCID 15294—
Reactant4-Tert-ButylanilineHCID 69861—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 39417231HCID 3941723199.8%

Reaction Steps

4-Formylbenzoic acid methyl ester (10.6 g, 64 mmol) was dissolved in methanol (200 ml). 4-tert-Butylaniline (9.61 g, 64 mmol) was added and the resulting suspension was refluxed for 15 minutes. After cooling to room temperature, TFA (5.18 ml, 68 mmol) was added followed by portion wise addition of sodium cyanoborohydride (3.26 g, 52 mmol). The resulting mixture was stirred at room temperature for 2 hours and concentrated in vacuo. The residue was partitioned between ethyl acetate (200 ml) and 1N aqueous sodium hydroxide (150 and 100 ml). The organic phase was dried (magnesium sulphate) and evaporated in vacuo to afford 19.0 g (99%) of 4-[(4-tert-butylphenylamino)methyl]benzoic acid methyl ester as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649641B2
Source datasetuspto-grants-2003_11
ORD IDord-e09e97edb6f4475cafd22e33a83614cc
Source noteuspto-grants-2003_11