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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycine methyl ester | HCID 69221 | — |
| Reactant | HCID 20264986 | HCID 20264986 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 3-[(methoxycarbonylmethyl)sulfamoyl]-5-trifluoromethyl-thiophene-2-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04544655 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-29a33628e32b4c348ac055b74d486807 |
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| Source note | uspto-grants-1985_10 |
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