Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463665Generated: October 29, 2026

Glycine methyl ester → Methyl 3-[(methoxycarbonylmethyl)sulfamoyl]-5-trifluoromethyl-thiophene-2-carboxylate

https://huagongshe.com/reaction/463665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine methyl esterHCID 69221—
ReactantHCID 20264986HCID 20264986—
SolventChloroformHCID 6212—
ProductMethyl 3-[(methoxycarbonylmethyl)sulfamoyl]-5-trifluoromethyl-thiophene-2-carboxylateHCID 16639955—

Reaction Steps

103.8 g of methyl 3-chlorosulfonyl-5-trifluoromethyl-thiophene-2-carboxylate are dissolved in 600 ml of chloroform, 68.05 g of freshly distilled methyl glycinate are added dropwise thereto in a manner such that the temperature does not exceed 30°, the mixture is stirred at room temperature for an additional 0.5 hour and then extracted three times with 200 ml of 1N hydrochloric acid each time. The organic phase is dried over sodium sulfate and evaporated. The oily residue is stirred with 175 ml of diisopropyl ether, and there is obtained methyl 3-[(methoxycarbonylmethyl)sulfamoyl]-5-trifluoromethyl-thiophene-2-carboxylate in the form of colorless crystals which are removed by filtration under suction and washed with diisopropyl ether. The product melts at 76°-78° after recrystallization from diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544655
Source datasetuspto-grants-1985_10
ORD IDord-29a33628e32b4c348ac055b74d486807
Source noteuspto-grants-1985_10