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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105841Generated: October 31, 2026

Ethyl Acetate → HCID 57809137, compound

https://huagongshe.com/reaction/2105841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68871137HCID 68871137—
SolventDichloromethaneHCID 6344—
ProductHCID 57809137HCID 5780913760.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled solution of ethyl 4-methylthio-2-ethoxybenzoate (1.1 g, 4.6 mmol) in methylene chloride (40 mL) was added 3-chloroperoxybenzoic acid (1.1 g, 4.5 mmol, 77%) in several portions. The reaction mixture was stirred at 0° C. for 15 min, after which TLC (50% ethyl acetate in hexanes) showed consumption of starting material. The reaction mixture was quenched with a solution of sodium thiosulfate and neutralize with a solution of sodium bicarbonate. The product was extracted three times with methylene chloride. The organic layer was washed with sodium bicarbonate, dried over magnesium sulfate, and concentrated. Purification of the crude residue by flash column chromatography (silica gel, eluting with 50% ethyl acetate in hexanes) gave ethyl 2-ethoxy-4-methanesulfinylbenzoate as a yellow oil (0.70 g, 58%). LC-MS: 257.2 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579368B2
Source datasetuspto-grants-2009_08
ORD IDord-ae22a6338e104dc483d43789ff28575a
Source noteuspto-grants-2009_08