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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365126Generated: October 27, 2026

Trifluoroacetic acid → Methyl 3-aminofuran-2-carboxylate

https://huagongshe.com/reaction/1365126

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 numberUS07888352B2
Source datasetuspto-grants-2011_02
ORD IDord-bafb474bb4ce498093ea9fdde0f5369a
Source noteuspto-grants-2011_02