HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369630Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 18516175, compound
https://huagongshe.com/reaction/1369630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 18516204 | HCID 18516204 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18516175 | HCID 18516175 | 90% |
Reaction Steps
To a stirred solution of oxalyl chloride (0.10 mL, 1.17 mmol) in anhydrous dichloromethane (1 mL) at −78° C. was added DMSO (0.19 mL, 2.65 mmol). After 20 minutes, a solution of dimethylethyl 4-(hydroxymethyl)-thieno[2,3-c]pyridine-2-carboxylate (0.28 g, 1.06 mmol) in anhydrous dichloromethane (4 mL) was added dropwise. The reaction was stirred 1 hours at −78° C. then treated with triethylamine (0.74 mL, 5.30 mmol). After 5 minutes, reaction was allowed to warm to room temperature over 30 minutes. The reaction was quenched with water (5 mL) and partitioned between dichloromethane (50 mL) and 50% sat. aq NaHCO3 (50 mL). The organic phase was washed with 50% sat. aq NaHCO3 (1×50 mL), dried (Na2SO4), filtered, and concentrated and dried in a desiccator to yield the title as a solid (0.25 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579882B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-042b2f2121804e35a409394709cfd2c7 |
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| Source note | uspto-grants-2003_06 |
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