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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257538Generated: November 2, 2026

Hydrochloric Acid → 1-Acetoxy-1-(3-chlorophenyl)-2-(2-methanesulfonyloxyethoxy)ethane

https://huagongshe.com/reaction/2257538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Acetoxy-1-(3-chlorophenyl)-2-(2-hydroxyethoxy)ethaneHCID 53790969—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1-Acetoxy-1-(3-chlorophenyl)-2-(2-methanesulfonyloxyethoxy)ethaneHCID 53684196—

Reaction Steps

To a mixture of 19.0 g of 1-acetoxy-1-(3-chlorophenyl)-2-(2-hydroxyethoxy)ethane and 95.0 ml of methylene chloride containing 9.1 ml of methanesulfonyl chloride was dropwise added 16.4 ml of triethylamine with ice cooling over 1 hour. The resulting mixture was stirred for 10 minutes at the same temperature and further for 1 hour at room temperature. The reaction mixture was added to a mixture of 50.0 ml of methylene chloride and 50.0 ml of ice water. The resulting mixture was adjusted to pH 2.0 with 6N hydrochloric acid. The organic layer was separated, washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 24.5 g of oily 1-acetoxy-1-(3-chlorophenyl)-2-(2-methanesulfonyloxyethoxy)ethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658904
Source datasetuspto-grants-1997_08
ORD IDord-1d6fab7831844162ba11f0ac5bea0d04
Source noteuspto-grants-1997_08