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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217437Generated: October 26, 2026

Sodium Thiosulfate → Methyl 5-bromo-4-phenylthiophene-2-carboxylate

https://huagongshe.com/reaction/217437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantMethyl 4-phenylthiophene-2-carboxylateHCID 2760021—
ReactantPyridiniumtribromideHCID 21124087—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-bromo-4-phenylthiophene-2-carboxylateHCID 5843885984.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of methyl 4-phenylthiophene-2-carboxylate (1.8 g) in DCM (18 mL) was added portionwise pyridinium tribromide (13.2 g) at 0° C. The reaction liquid was warmed to 25° C. and then stirred for 45 hours. The reaction mixture was cooled to 0° C., and a saturated aqueous Na2S2O3 solution (100 mL) was slowly added dropwise. The reaction mixture was extracted with DCM (50 mL) three times. The organic layer was washed with brine, dried over MgSO4, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=100:0 to 90:10) to obtain methyl 5-bromo-4-phenylthiophene-2-carboxylate (2.06 g) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-2262549147284e38ab6c476f16639f00
Source noteuspto-grants-2012_06