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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305339Generated: November 1, 2026

Hydrochloric Acid → HCID 59905801, compound

https://huagongshe.com/reaction/2305339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantHCID 11091303HCID 11091303—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59905801HCID 5990580186%

Reaction Conditions

Temperature-30 °C

Reaction Steps

In a 250 mL dry RB flask, 4.50 mL of TiCl4 (40.8 mmol) was dissolved in 100 mL of CH2Cl2 and was cooled to −30° C. A solution of 2-[methoxycarbonyl-methyl-(2-trifluoromethyl-phenyl)-sulfamoyl]-benzoic acid methyl ester (8.0 g, 18.54 mmol) in 50 mL CH2Cl2 was added dropwise. The resulting solution was kept at −30° C. for 30 minutes and was then cooled to −78° C. Et3N (7.75 mL, 55.6 mmol) in 50 mL CH2Cl2 was slowly syringed in resulting a dark red solution. The reaction mixture was stirred at −78° C. for 4 hours and was then poured into a 1-L flask containing 250 mL of Et2O, 100 mL concentrated HCl, and 100 mL of H2O. The mixture was stirred at room temperature overnight. The layers were separated, and the organic layer was washed with brine and dried over MgSO4. Upon evaporation of the solvent, light yellowish crystals of 4-hydroxy-1,1-dioxo-2-(2-trifluoromethyl-phenyl)-1,2-dihydro-1λ6-benzo[e][1,2]thiazine-3-carboxylic acid methyl ester were formed. The product was collected through filtration and dried in oven to provide 2.2 g, 86% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440962B2
Source datasetuspto-grants-2002_08
ORD IDord-47ad630fb9ca4fc6b388599345ab85f1
Source noteuspto-grants-2002_08