HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217436Generated: October 29, 2026
Methanol → Methyl 4-bromo-5-ethylthiophene-2-carboxylate
https://huagongshe.com/reaction/217436
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Bromo-5-ethylthiophene-2-carboxylic acid | HCID 3766372 | — |
| Product | Methyl 4-bromo-5-ethylthiophene-2-carboxylate | HCID 57826917 | — |
Reaction Steps
The suspension of 4-bromo-5-ethylthiophene-2-carboxylic acid (800 mg) in MeOH (4 mL) was added dropwise SOCl2 (0.50 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour, warmed to 60° C., and then stirred for 15 hours. The reaction liquid was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=98:2 to 70:30) to obtain methyl 4-bromo-5-ethylthiophene-2-carboxylate (765.0 mg) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193378B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-22af2f5622c6457db064bd64a56613b4 |
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| Source note | uspto-grants-2012_06 |
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