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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914284Generated: November 2, 2026

Hydrochloric Acid → HCID 54330522, compound

https://huagongshe.com/reaction/1914284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86615984HCID 86615984—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 54330522HCID 54330522—

Reaction Steps

Dimethyl-thiocarbamic acid S-(4-bromo-3,5-dimethyl-phenyl) ester (5.78 g, 20.14 mmol) is diluted with methanol (50 mL) and sodium methoxide (4.75 mL of 4.25M in methanol, 20.14 mmol) is added. The reaction is heated to reflux under nitrogen and monitored by TLC. After complete conversion, 20 hours, the reaction is allowed to cool to room temperature. The reaction is neutralized with 1N hydrochloric acid (7.5 mL) and diluted with ethyl acetate (150 mL). The two phases are separated and the organic layer is washed with water (75 mL), then brine (75 mL). The organic layer is dried over anhydrous sodium sulfate, concentrated and loaded onto silica gel column. The title compound is purified using flash column chromatography, yielding 4.0 g, or 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609892B2
Source datasetuspto-grants-2013_12
ORD IDord-7ed5b7c8432a49e3874f5a2771f9a065
Source noteuspto-grants-2013_12