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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490228Generated: October 26, 2026

Thionyl Chloride → HCID 21480612, compound

https://huagongshe.com/reaction/1490228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantPiperidin-4-olHCID 79341—
Reactant9,10-Dihydro-9,10-methano-9-anthracenecarboxylic acidHCID 12507119—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 21480612HCID 21480612—

Reaction Steps

To a solution of 9,10-dihydro-9,10-methano-9-anthracenecarboxylic acid (24.1 mmol) in toluene (70 mL) was added thionyl chloride (2.28 mL, 31.3 mmol, 1.3 eq). The reaction was heated to reflux monitoring gas evolution with a mineral oil bubbler. The system reached a steady state within 40 min at which time it was slightly cooled and 4-hydroxypiperidine (6.08 g, 60.3 mmol, 2.5 eq) was added portionwise. A significant amount of heat is evolved and the reaction became dark. The suspension was heated to reflux for 2 h, cooled to room temperature and stirred for 18 h. The reaction was diluted with ethyl acetate (200 mL) and washed with 3N HCl (2×100 mL), 2.5N NaOH (2×100 mL) and saturated brine (200 mL). The organic phase was dried over anhydrous magnesium sulfate, filtered, and reduced to an oil. The procedure yielded the title compound in quantitative yield as a viscous oil. TLC analysis (Rf 0.54, 10% methanol in CHCl3). MS (Cl, CH4) m/z 320 (M+1, 100), 348 (M+29,22), 302 (16)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681840
Source datasetuspto-grants-1997_10
ORD IDord-fa23f22e8065440fb5cb4e2072fa522a
Source noteuspto-grants-1997_10