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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131281Generated: November 2, 2026

Benzocaine → Ethyl 4-(methylamino)benzoate

https://huagongshe.com/reaction/131281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl orthoformateHCID 31214—
ProductEthyl 4-(methylamino)benzoateHCID 31983246.5%

Reaction Steps

A mixture of ethyl p-aminobenzoate (25.2 g), triethyl orthoformate (80 g) and trifluoroacetic acid (0.2 mL) is refluxed under heating for 3 hours. After cooling, the reaction mixture is concentrated in vacuo and the residue is subjected to azeotropic distillation with ethanol. The residue is suspended in ethanol (400 mL) and thereto is added sodium borohydride (23 g), and the mixture is refluxed under heating for 3 hours. After cooling, to the reaction mixture is added ethyl acetate and water. The mixture is stirred at room temperature for 1 day. The organic layer is separated, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue is purified by flash column chromatography on silica gel (Solvent; n-hexane:ethyl acetate=4:1) to give ethyl 4-(methylamino)benzoate (12.7 g, yield; 46%) as a pale yellow amorphous powder. MS (APCI) m/z: 180 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384952B2
Source datasetuspto-grants-2008_06
ORD IDord-853a5d7c97b146f192ea38a022e62efb
Source noteuspto-grants-2008_06