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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518286Generated: November 3, 2026

Dimethyl Sulfate → HCID 59447591, compound

https://huagongshe.com/reaction/1518286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantSodium BicarbonateHCID 516892—
Reactant4-BenzyloxybenzoylmalononitrileHCID 22169785—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59447591HCID 5944759179.7%

Reaction Steps

Compound 31B (3.7 g, 13.39 mmol) was dissolved in 1,4-dioxane (30 mL) and water (5 mL). To this solution was added to sodium bicarbonate (9.0 g, 107 mmol) portionwise to control the gas formation. To the resulting suspension was added dimethyl sulfate (8.96 mL, 94 mmol). The reaction was heated under reflux for 2 hours. The reaction mixture was concentrated, and partitioned between water and EtOAc. The aqueous layer was extracted with additional EtOAc. The combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel eluting with 7:3/hexanes: EtOAc to provide 3.1 g of the desired product: 1H NMR (DMSO-d6): δ 7.64-7.68 (m, 2H), 7.34-7.69 (m, 5H), 7.22-7.26 (m, 2H), 5.22 (s, 2H), 3.92 (s, 3H). MS (DCI(+)): m/z 308 (M+NH4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232273B2
Source datasetuspto-grants-2012_07
ORD IDord-ce3ca0697eca4c82b0fde11bbb39add1
Source noteuspto-grants-2012_07