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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390810Generated: October 26, 2026

Trifluoroacetic acid → Methyl 3-aminofuran-2-carboxylate

https://huagongshe.com/reaction/390810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 3-((tert-butoxycarbonyl)amino)furan-2-carboxylateHCID 52987670—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-aminofuran-2-carboxylateHCID 4579012086.1%

Reaction Steps

Tert-butyl 2-(methoxycarbonyl)furan-3-ylcarbamate 33 (1.14 g, 1.0 eq) was dissolved in dichloromethane (8 ml) and treated with trifluoroacetic acid (5 ml). Reaction mixture was stirred at room temperature for 3 h, and was then concentrated. Residue was dissolved in dichloromethane and washed with saturated aq. NaHCO3. The organic layer was dried (Na2SO4) and concentrated Mixture was extracted with ethyl acetate. The combined organic extracts were dried with Na2SO4 and concentrated. The crude reaction mixture was purified by flash chromatography to yield methyl 3-aminofuran-2-carboxylate 34 (574 mg, 86%): MS (Q1) 142 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383620B2
Source datasetuspto-grants-2013_02
ORD IDord-c57c55defa9c4334889be0fb5fb5d5d9
Source noteuspto-grants-2013_02