HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492928Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 53927843, compound
https://huagongshe.com/reaction/1492928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53960446 | HCID 53960446 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53927843 | HCID 53927843 | — |
Reaction Steps
A mixture of 2 g of methyl α-(5-bromomethyl-3-benzo[b]thienyl)-13-methoxyacrylate (see Example 11), 16 ml of dimethyl sulfoxide and 0.5 g of sodium hydrogencarbonate is heated at 85° C. for 2.5 hours. Water is subsequently added, and the mixture is extracted using ethyl acetate. The organic phase is dried over anhydrous sodium sulfate and concentrated under reduced pressure, and the residue is then purified by chromatography on silica gel using diethyl ether/n-hexane (2:1). Recrystallization from methylene chloride/n-hexane gives methyl α-(5-formyl-3-benzo[b]thienyl)-β-methoxyacrylate as colourless crystals, m.p. 134°-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05376677 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-3ec4399c58784aa994322e85cfff6ba6 |
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| Source note | uspto-grants-1994_12 |
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