HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68232Generated: October 29, 2026
Dimethyl Sulfate → HCID 12763272, compound
https://huagongshe.com/reaction/68232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3-Benzenedithiol | HCID 522062 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 12763272 | HCID 12763272 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822439B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-62a5d83b7c594413a7da477ba5532a08 |
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| Source note | uspto-grants-2014_09 |
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