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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881235Generated: October 26, 2026

Trifluoroacetic acid → Methyl 3-aminofuran-2-carboxylate

https://huagongshe.com/reaction/881235

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 numberUS08993563B2
Source datasetuspto-grants-2015_03
ORD IDord-da8b7ac855eb4f1198521eb7eea22ca4
Source noteuspto-grants-2015_03