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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]-5-(hydroxymethyl)azepan-2-oneHCID 86678801—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1-[2,4-Bis(trifluoromethyl)benzyl]-7-oxoazepane-4-carbaldehydeHCID 8667880246.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-fe932f345f2d47a3bc7fd82c2e807935
Source noteuspto-grants-2014_07