HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611406Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 19599906, compound
https://huagongshe.com/reaction/611406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19600247 | HCID 19600247 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19599906 | HCID 19599906 | — |
Reaction Steps
To a solution of 0.16 ml (1.2 mmol) of oxalyl chloride in 30 ml of dichloromethane, 0.17 ml (2.5 mmol) of dimethyl sulfoxide was added dropwise at -78° C., followed by stirring for 5 minutes. To the solution, a solution of 0.303 g (0.820 mmol) of 4-(6,7-dihydro-4H-furo[3,2-c]pyridin-5-ylsulfonyl)phenylphenylmethanol in 10 ml of dichloromethane was added at -78° C., followed by stirring for 15 minutes. To this mixture, 0.69 ml (4.9 mmol) of triethylamine was added; the mixture was allowed to warm to room temperature. After the reaction mixture was washed with water, the water layer was re-extracted with diethyl ether. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=3/1) and washed with diethyl ether-hexane to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998433 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-e3dbe153951d4ea587bbaca1ee9dd350 |
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| Source note | uspto-grants-1999_12 |
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