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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215738Generated: October 30, 2026

Ethyl chloroformate → Methyl 3-((ethoxycarbonyl)amino)thiophene-2-carboxylate

https://huagongshe.com/reaction/215738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
SolventBenzeneHCID 241—
ProductMethyl 3-((ethoxycarbonyl)amino)thiophene-2-carboxylateHCID 84018198.4%

Reaction Steps

To a solution of 3-amino-thiophene-2-carboxylic acid methyl ester (2.39 g, 15.2 mmol) in benzene (51 mL) was added K2CO3 (6.30 g, 45.6 mmol) followed by ethyl chloroformate (1.74 mL, 18.2 mmol). After heating at reflux for 12 h, the mixture was filtered and the filtrate was concentrated to afford the desired product (3.43 g), which was used in the next step without further purification. MS: 230.0. 1H NMR (400 MHz, CD3OD) δ ppm 7.82 (d, J=5.5 Hz, 1H), 7.66 (d, J=5.6 Hz, 1H), 4.23 (q, J=7.1 Hz, 2H), 3.86 (s, 3H), 1.32 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193178B2
Source datasetuspto-grants-2012_06
ORD IDord-2c01ccd83eff4bcabc75c1757047dc50
Source noteuspto-grants-2012_06