Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78492Generated: October 27, 2026

Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → Methyl 5-chloro-2-(2-chloroethoxy)benzoate

https://huagongshe.com/reaction/78492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 2-chloro-, 1-(4-methylbenzenesulfonate)HCID 6639—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoic acid, 5-chloro-2-hydroxy-, methyl esterHCID 77684—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-chloro-2-(2-chloroethoxy)benzoateHCID 66846837—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of methyl-5-chlorosalicylate (19.5 g, 105 mmol), 2-chloroethyl p-toluenesulfonate (19.3 mL, 107 mmol) and K2CO3 (28.9 g, 210 mmol) in 105 mL of N,N-dimethylformamide was warmed to 50° C. and allowed to stir for 18 hours. The mixture was cooled to ambient temperature, diluted with 25 mL of ethyl acetate and 25 mL of H2O. The layers were separated and the organic layer was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification via column chromatography (SiO2, 75% hexanes in ethyl acetate) afforded the title compound. MS (DCI/NH3) m/z 249 (M+H)+, 266 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841334B2
Source datasetuspto-grants-2014_09
ORD IDord-191942b1cd1f4610a6c345a57cd8f0b7
Source noteuspto-grants-2014_09