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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967640Generated: October 30, 2026

Trifluoroacetic acid → HCID 39417231, compound

https://huagongshe.com/reaction/967640

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 min. 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 1 N 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 numberUS06953812B2
Source datasetuspto-grants-2005_10
ORD IDord-615fa7ac21934c1bbbdff7376cc63068
Source noteuspto-grants-2005_10