HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620635Generated: November 1, 2026
Dimethyl Sulfoxide → 1-[2,4-Bis(trifluoromethyl)benzyl]-7-oxoazepane-4-carbaldehyde
https://huagongshe.com/reaction/1620635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-[2,4-Bis(trifluoromethyl)benzyl]-5-(hydroxymethyl)azepan-2-one | HCID 86678801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-[2,4-Bis(trifluoromethyl)benzyl]-7-oxoazepane-4-carbaldehyde | HCID 86678802 | 46.3% |
Reaction Steps
To a solution of DMSO (1.40 g) in dichloromethane (100 mL) was slowly added a solution of oxalyl chloride (2.48 g) in dichloromethane (200 mL) at −78° C. The reaction mixture was stirred for 5 min, a solution of 1-[2,4-bis(trifluoromethyl)benzyl]-5-(hydroxymethyl)azepan-2-one (6.0 g) in dichloromethane (100 mL) was added dropwise, and the mixture was stirred for 15 min. Triethylamine (8.2 g) was added and the mixture was allowed to warm to room temperature. Saturated aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether) to give the title compound (2.76 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772277B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-fe932f345f2d47a3bc7fd82c2e807935 |
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| Source note | uspto-grants-2014_07 |
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