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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709442Generated: October 29, 2026

Ethyl Acetate → S-[2-[4-[(Methylsulfonyl)oxy]phenyl]ethyl] ethanethioate

https://huagongshe.com/reaction/709442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant1-(Methylsulfonyloxy)-2-[4-(methylsulfonyloxy)phenyl]ethaneHCID 11220122—
ReactantHCID 178418634HCID 178418634—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductS-[2-[4-[(Methylsulfonyl)oxy]phenyl]ethyl] ethanethioateHCID 86650296—

Reaction Steps

Thioacetic acid (0.28 g, 3.73 mmol) was dissolved in anhydrous MeOH (3 mL) and Cs2CO3 (1.10 g, 3.39 mmol) was added. After 15 min. stirring at room temperature the MeOH evaporated under reduced pressure and the remaining oil was redissolved in anhydrous DMF (3 ml). Methanesulfonic acid 4-(2-methanesulfonyloxy-ethyl)-phenyl ester (1.00 g, 3.39 mmol), dissolved in anhydrous DMF (2 mL) was added dropwise and the reaction was stirred at room temperature for 4 h. Additional thioacetic acid (0.14 g, 1.86 mmol) was added to the reaction mixture. After 30 min. stirring, the mixture was partioned between EtOAc and brine. The separated organic layer was dried (Na2SO4) and finally concentration under reduced pressure. The crude material was purified by flash chromatography on silica gel 60 using n-heptan/EtOAc 7:3 as the eluent to afford the title compound as an oil. 1H NMR (400 MHz, CDCl3): δ 7.17-7.25 (m, 4H), 3.10 (s, 3H), 3.05-3.08 (t, 2H), 2.83-2.86 (t, 2H), 2.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181181B2
Source datasetuspto-grants-2015_11
ORD IDord-1d3135f0ac914551bda2237c4b896668
Source noteuspto-grants-2015_11