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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390789Generated: October 26, 2026

Ethyl Thioglycolate → (2,4-Dichloro-phenoxymethylsulfanyl)-acetic acid

https://huagongshe.com/reaction/390789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium hydrideHCID 24758—
ReactantChloromethyl 2,4-dichlorophenyl etherHCID 12353529—
SolventDimethylformamideHCID 6228—
Product(2,4-Dichloro-phenoxymethylsulfanyl)-acetic acidHCID 6857933457%

Reaction Steps

To a solution of mercapto-acetic acid ethyl ester (2.4 g, 19.86 mmol) in dry DMF (20 mL) was added NaH (556 mg, 23.27 mmol, 60% in mineral oil). The mixture was stirred for 30 min. at room temperature followed by dropwise addition of 2,4-dichloro-1-chloromethoxy-benzene (3.5 g, 16.55 mmol), stirring was continued for 16 hrs at ambient temperature. The reaction was quenched by addition of water (50 mL) and extracted with diethyl ether (2×50 mL). The combined organic phases were washed with saturated aq. ammonium chloride (50 mL), dried (Na2SO4), filtered and evaporated in vacuo. The residue was dissolved in EtOH (20 mL) and to this solution was added aq. 32% NaOH (1 mL) and water (10 mL). Stirring was continued for 16 hrs at room temperature. The volatiles were evaporated in vacuo, water (20 mL) was added followed by washing with diethyl ether (20 mL). The aqueous phase was acidified to pH˜1 with conc. HCl followed by extraction with diethyl ether (2×25 mL). The combined organic phases were dried (Na2SO4), filtered and the solvent evaporated in vacuo affording 2.5 g (57%) of crude (2,4-dichloro-phenoxymethylsulfanyl)-acetic acid as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383683B2
Source datasetuspto-grants-2013_02
ORD IDord-a453e45a758147478180b7c069703a00
Source noteuspto-grants-2013_02