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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717540Generated: October 29, 2026

Dimethyl Sulfide → HCID 89463002, compound

https://huagongshe.com/reaction/717540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantPhenyl chloroformateHCID 15891—
Reactant3-Bromo-5-fluoropyridineHCID 820206—
ReactantHCID 178418630HCID 178418630—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89463002HCID 89463002—

Reaction Steps

Phenyl chloroformate (4.2 mL, 0.033 mol) was added to a mixture of 3-bromo-5-fluoro-pyridine (5.5 g, 0.031 mol), dimethyl sulphide (15.32 mL, 0.209 mol) and copper iodide (5.95 g, 0.031 mol) in anhydrous tetrahydrofuran (50 mL) at RT and the reaction mixture was stirred for 40-50 min. To this suspension, cyclopropylmagnesiumbromide (66.75 mL, 0.033 mol, 0.5 M solution in tetrahydrofuran) was added at −25 to −20° C. over a 30-40 min period. The mixture was stirred at this temperature for 30 min, and then warmed slowly to RT over 1.0-1.5 hrs. The reaction mixture was quenched with a saturated aqueous ammonium chloride solution (200 mL), followed by extraction of the aqueous layer with ethyl acetate (3×200 mL). The combined organic layers were washed with a saturated aqueous sodium chloride solution (2×100 mL), and dried over anhydrous sodium sulphate to afford the crude compound, which was purified by silica gel chromatography using 0-5% ethyl acetate-hexane gradient. This yielded crude phenyl 3-bromo-4-cyclopropyl-5-fluoro-4H-pyridine-1-carboxylic acid phenyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193724B2
Source datasetuspto-grants-2015_11
ORD IDord-cc5084c651f34f908a3e5e9ce1bb2f5e
Source noteuspto-grants-2015_11