HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807906Generated: October 30, 2026
Dimethyl Sulfoxide → 2-(4-Fluorophenyl)-2-methylpropanal
https://huagongshe.com/reaction/1807906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(4-Fluorophenyl)-2-methylpropan-1-ol | HCID 21262802 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Fluorophenyl)-2-methylpropanal | HCID 82074750 | — |
Reaction Steps
To a stirred solution of oxalyl chloride (2.81 ml) in dichoromethane (30 ml) at −60° C. was added dropwise a solution of dry dimethyl sulphoxide (4.84 ml) in dichloromethane (20 ml). The mixture was stirred for 15 min at −60° C. and then a solution of 2-(4-fluoro-phenyl)-2-methyl-propan-1-ol (4.59 g; CAS 703-10-6) in dichloromethane (20 ml) was added dropwise. The mixture was stirred at −60° C. for 2 hours and then triethylamine (18.9 ml) was added dropwise. The reaction mixture was allowed to warm to room temperature and diluted with water and with dichloromethane. The phases were separated and the organic phase was washed with water and then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc gradient) to yield a colourless oil, (3.47 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357712B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-fb928b76fc3b413d964918a05317227a |
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| Source note | uspto-grants-2013_01 |
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