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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902481Generated: November 1, 2026

Ethanol → HCID 2807589, compound

https://huagongshe.com/reaction/902481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPyridineHCID 1049—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
Reactant2-Ethylpropanedioyl dichlorideHCID 10920924—
SolventTolueneHCID 1140—
ProductHCID 2807589HCID 280758963%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Ethylmalonyl chloride (1.93 mL, 15.22 mmol) was added to a solution of methyl-3-amino-thiophene-2-carboxylate (2 g, 12.70 mmol) in dry toluene (20 mL) and pyridine (1.23 mL, 15.22 mmol) at −10° C. The solution was stirred at −10° C. for 1 h and poured into ice water. The product was extracted by ethyl acetate. The combined organic phase was sequentially washed by diluted HCl solution, saturated NaHCO3 solution, water, and brine. The organic phase was dried over MgSO4 and concentrated to yield an oily residue. The residue was dissolved in hot ethanol and kept overnight at −4° C. The crystals formed were filtered off and filtrate was concentrated to yield 2.2 g (63%) of 3-(2-ethoxycarbonyl-acetylamino)-thiophene-2-carboxylic acid methyl ester as yellow viscous oil. 1H NMR (400 MHz, DMSO-d6) δ 1.21 (t, J=7.2 Hz, 3H), 3.68 (s, 2H), 3.84 (s, 3H), 4.15 (q, J=7.2 Hz, 2H), 7.91 (d, J=5.2 Hz, 1H), 7.93 (d, J=5.2 Hz, 1H), 10.52 (s, 1H) ppm; MS m/z=272 amu (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365200B2
Source datasetuspto-grants-2008_04
ORD IDord-fad71b9a9abb41ec90e461a56961e6d9
Source noteuspto-grants-2008_04