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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243552Generated: October 26, 2026

Hydrochloric Acid → Ethyl 4'-(2-methanesulfonyloxyethoxy)biphenyl-4-carboxylate

https://huagongshe.com/reaction/2243552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 4'-(2-hydroxyethoxy)biphenyl-4-carboxylateHCID 23090738—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4'-(2-methanesulfonyloxyethoxy)biphenyl-4-carboxylateHCID 23090736—

Reaction Steps

Methanesulfonyl chloride (0.13 mL) was added to an ice-cooled mixture of ethyl 4′-(2-hydroxyethoxy)biphenyl-4-carboxylate (0.41 g) and triethylamine (0.30 mL) in tetra hydrofuran (8 mL) with stirring. The mixture was stirred at that temperature for 30 min, at room temperature for 45 min, and at 45° C. for 1 hr. Methanesulfonyl chloride (0.13 mL) and triethylamine (0.30 mL) were added every an hour to the reaction mixture for 3 times at 45° C., and the mixture was stirred at 70° C. for 3 hrs. 1 mol/L hydrochloric acid and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over an hydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford ethyl 4′-(2-methanesulfonyloxyethoxy)biphenyl-4-carboxylate (0.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674938B2
Source datasetuspto-grants-2010_03
ORD IDord-81292a73c81c427a95e11ce3228c2ff4
Source noteuspto-grants-2010_03