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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860636Generated: October 31, 2026

Water → Ethyl (4-mercapto-2-methylphenoxy)acetate

https://huagongshe.com/reaction/860636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichlorodimethylsilaneHCID 6398—
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantEthyl 4-chlorosulfonyl-2-methylphenoxyacetateHCID 11415129—
CatalystZincHCID 23994—
Solvent1,2-DichloroethaneHCID 11—
Solvent1,1-DichloroethaneHCID 6365—
ProductEthyl (4-mercapto-2-methylphenoxy)acetateHCID 16641178—

Reaction Conditions

Temperature52 °C

Reaction Steps

This compound can also be made by the following procedure: To a stirred suspension of Zn powder (10 μm, 78.16 g, 1.2 mol) and dichlorodimethyl silane (154.30 g, 145.02 mL, 1.2 mol) in 500 mL of dichloroethane is added a solution of (4-chlorosulfonyl-2-methyl-phenoxy)-acetic acid ethyl ester (100 g, 0.34 mol) and 1,3-dimethylimidazolidin-2-one (116.98 g, 112.05 mL, 1.02 mol) in 1 L of DCE. Addition is at a rate so as to maintain the internal temperature at ˜52° C., cooling with chilled water as necessary. After addition is complete, the mixture is heated at 75° C. for 1 hour. It is then cooled to room temperature, filtered and concentrated iv. Add MTBE, washed twice with saturated LiCl solution concentrate iv again. Take up the residue in CH3CN, ish with hexane (4×) and concentrate iv to yield a biphasic mixture. Let stand in a separatory funnel and separate layers, keeping the bottom layer for product. Filtration through a plug of silica gel (1 Kg, 25% EtOAc/hexane) and subsequent concentration yielded 61 g (79%) of a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153878B2
Source datasetuspto-grants-2006_12
ORD IDord-2872b492a9574bfa98b5e742feb526f7
Source noteuspto-grants-2006_12