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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721805Generated: November 1, 2026

Dimethyl Sulfoxide → (9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinone

https://huagongshe.com/reaction/1721805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)piperidin-4-olHCID 21480617—
SolventDichloromethaneHCID 6344—
Product(9,10-Dihydro-9,10-methanoanthracen-9-ylmethyl)-4-piperidinoneHCID 2148060580%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cooled solution (-78° C.) of oxalyl chloride (3.06 mL, 35.1 mmol, 2 eq) in methylene chloride (100 mL) under nitrogen was added distilled dimethylsulfoxide (5.00 mL, 70.2 mmol, 4 eq). After 10 min 1-(9,10-dihydro-9,10-methanoanthracen-9-ylmethyl) piperidin-4-ol (described above) (17.5 mmol) was added as a methylene chloride solution (10 mL). The reaction was stirred at -78° C. for 30 min prior to the addition of triethylamine (19.6 mL, 140 mmol, 8 eq). The cooling bath was removed and the reaction warmed to room temperature over 1.5 h. The reaction mixture was poured into 2.5N NaOH (100 mL) and the aqueous phase extracted with methylene chloride (3×100 mL). Combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and reduced to an oil. The crude reaction mixture was purified by flash chromatography over silica gel (400 mL, eluent:20% ethyl acetate in hexane) to yield the title compound in 80% yield as a white solid. TLC analysis (Rf 0.31, 2% methanol in methylene chloride). MS (Cl, CH4) m/z 304 (M+1,100), 332 (M+29,21)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512575
Source datasetuspto-grants-1996_04
ORD IDord-63cfe6a4909b4b04a425716fc112625e
Source noteuspto-grants-1996_04