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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Methyl 4-phenylthiophene-2-carboxylate | HCID 2760021 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-bromo-4-phenylthiophene-2-carboxylate | HCID 58438859 | 84.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08193378B2 |
|---|
| Source dataset | uspto-grants-2012_06 |
|---|
| ORD ID | ord-2262549147284e38ab6c476f16639f00 |
|---|
| Source note | uspto-grants-2012_06 |
|---|