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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914856Generated: October 25, 2026

Dimethyl Sulfoxide → (1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanone

https://huagongshe.com/reaction/914856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanolHCID 22248465—
SolventDichloromethaneHCID 6344—
Product(1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanoneHCID 2224814487.1%

Reaction Steps

After adding 0.511 ml of dimethylsulfoxide dropwise to a dichloromethane solution (15 ml) containing 0.315 ml of oxalyl chloride at −70° C., the mixture was stirred for 10 minutes, a solution of 597 mg of (1-benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanol in dichloromethane (5 ml) was added dropwise, and stirring was continued for 1 hour. Next, 2.5 ml of triethylamine was added dropwise to the reaction solution, the cooling bath was removed, and the mixture was stirred at room temperature. Water was added to the reaction solution, and extraction was performed with ethyl acetate. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to obtain the title compound (517 mg, 33% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265108B2
Source datasetuspto-grants-2007_09
ORD IDord-a3d861881ba347609a29246b82287887
Source noteuspto-grants-2007_09