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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352048Generated: November 1, 2026

Ethyl Acetate → (R)-4-(Methylthio)-2-(methanesulfonyloxy)butyl Methanesulfonate

https://huagongshe.com/reaction/2352048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(R)-4-(methylthio)1,2-butanediolHCID 10920564—
SolventPyridineHCID 1049—
Product(R)-4-(Methylthio)-2-(methanesulfonyloxy)butyl MethanesulfonateHCID 14634096—

Reaction Conditions

Temperature0 °C

Reaction Steps

(R)-4-(Methylthio)-1,2-butanediol (0.47 g, 3.4 mmol) was dissolved in 5 ml of pyridine and cooled to 0° C. Methanesulfonyl chloride (0.66 ml, 8.5 mmol) was added and the mixture stirred for 2 hours while warming to room temperature, by which time tlc (ethyl acetate) indicated complete conversion of starting material (Rf 0.4) to title product (Rf 0.85). The reaction mixture was diluted with 10 ml H2O and extracted 2×15 ml of ethyl acetate. The organic layers were combined, dried (MgSO4) and stripped to in vacuo to yield title product an an oil, all of which was used in the next step; tlc Rf 0.85 (ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874877
Source datasetuspto-grants-1989_10
ORD IDord-532610ed14bf403295b4dde4c4f0ed47
Source noteuspto-grants-1989_10