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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402827Generated: October 25, 2026

4-Methylmorpholine → Methyl 3,5-dibromo-4-{[(phenylsulfanyl)carbonothioyl]oxy}benzoate

https://huagongshe.com/reaction/402827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPhenyl ChlorodithioformateHCID 592675—
ReactantMethyl 3,5-dibromo-4-hydroxybenzoateHCID 726975—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3,5-dibromo-4-{[(phenylsulfanyl)carbonothioyl]oxy}benzoateHCID 7723087499.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl 3,5-dibromo-4-hydroxybenzoate (1000 mg, 3.23 mmol) was dissolved in THF (16 mL) and N-methylmorpholine (0.709 mL, 6.45 mmol) was added. The mixture was cooled to 0° C. and phenyl chlorodithioformate (0.549 mL, 3.87 mmol) was added. The mixture was warmed to room temperature and stirred overnight. The mixture was diluted with EtOAc and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography (0-15% EtOAc/hexanes) to yield the title compound as a clear oil (1491 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742110B2
Source datasetuspto-grants-2014_06
ORD IDord-719259b39ba4474b81d51115e00d21d3
Source noteuspto-grants-2014_06