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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707463Generated: October 29, 2026

Hydrochloric Acid → HCID 14015025, compound

https://huagongshe.com/reaction/707463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4-oxo-4,5-dihydrothiophene-3-carbonitrileHCID 13548092—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 14015025HCID 14015025166.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

Methyl chloroformate (55 g, 0.58 mol) was added to a stirred solution of 2-amino-4-oxo-4,5-dihydrothiophene-3-carbonitrile (68 g, 0.49 mol) and triethylamine (147 g, 1.45 mol) in dichloromethane (1000 ml) at 0° C. After the addition, the mixture was warmed to 25° C. and stirred overnight. The reaction was treated with dichloromethane-methanol (20:1, 2000 mL) and 2N hydrochloric acid (1500 mL). The resulting mixture was filtered and the resulting solid was further extracted with dichloromethane-methanol (20:1, 1500 mL×3). The combined organic extracts were dried over sodium sulfate and concentrated to give a brown solid. The solid was washed with tert-butyl methyl ether (1500 mL) and dried under vacuum to give crude methyl 3-cyano-4-methylthiophen-2-ylcarbamate (160 g) as a brown solid, which was used in next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175010B2
Source datasetuspto-grants-2015_11
ORD IDord-3205d3df458548029281a21019f0018c
Source noteuspto-grants-2015_11