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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68232Generated: October 29, 2026

Dimethyl Sulfate → HCID 12763272, compound

https://huagongshe.com/reaction/68232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantSodium HydroxideHCID 14798—
Reactant1,3-BenzenedithiolHCID 522062—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 12763272HCID 1276327278%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of benzene-1,3-dithiol (50 g, 0.351 mmol) in 2-methyltetrahydrofuran (375 mL, 0.351 mmol) was treated with dimethylsulfate (33.3 mL, 0.351 mol) followed by 2-methyltetrahydrofuran (25 mL, used as line wash). The resulting solution was cooled to between 0° C. and 5° C. and sodium hydroxide (2M aqueous solution, 210.6 mL) was added drop wise maintaining the temperature of the reaction mixture below 15° C. followed by 2-methyltetrahydrofuran (25 mL, used as line wash) and heated under nitrogen to 50° C. for 4 hours. After cooling to ambient temperature the resulting solution was treated with tert-butylmethylether (500 mL) and the phases were separated. The organic phase was extracted with sodium hydroxide (2 M aqueous solution, 250 mL) and the combined aqueous phases were cooled to 10° C. and hydrochloric acid (6M aqueous solution, 500 mL) was added whilst maintaining the temperature of the mixture below 25° C. The resulting solution was extracted with tert-butylmethylether (2-fold 250 mL) and the combined organic phases were washed with water (500 mL) and concentrated in vacuo to give the title compound as a yellow oil, 78% yield, 42.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822439B2
Source datasetuspto-grants-2014_09
ORD IDord-62a5d83b7c594413a7da477ba5532a08
Source noteuspto-grants-2014_09