HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131281Generated: November 2, 2026
Benzocaine → Ethyl 4-(methylamino)benzoate
https://huagongshe.com/reaction/131281
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Product | Ethyl 4-(methylamino)benzoate | HCID 319832 | 46.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384952B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-853a5d7c97b146f192ea38a022e62efb |
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| Source note | uspto-grants-2008_06 |
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