HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987781Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 23118281, compound
https://huagongshe.com/reaction/1987781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 23118299 | HCID 23118299 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23118281 | HCID 23118281 | 87.8% |
Reaction Steps
Under a nitrogen flow at −60° C., 1.6 ml of oxalic acid dichloride was dissolved in 40 ml of methylene chloride and 3.1 ml of DMSO was added dropwise at −60° C., followed by stirring for 5 minutes. A solution prepared by dissolving 3.9 g of 6-nitro-2-hydroxymethyl-2,5,7,8-tetramethylchroman in 10 ml of methylene chloride was added dropwise under a nitrogen gas flow at −60° C., followed by stirring at −60° C. for 30 minutes. 12 ml of triethylamine was added at −60° C. and the temperature was gradually raised to room temperature, thereby to complete the reaction. After the completion of the reaction, the reaction solution was poured into water and then extracted with chloroform. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. After removing magnesium sulfate by filtration and concentrating under reduced pressure, the residue was subjected to silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain 3.4 g of the objective product as a crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07553837B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-d91ecb9cd9324893bf9bc498adb35da4 |
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| Source note | uspto-grants-2009_06 |
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