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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394338Generated: November 1, 2026

Thioanisole → HCID 18538495, compound

https://huagongshe.com/reaction/1394338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 18538495HCID 1853849582.4%

Reaction Steps

To a stirred suspension of aluminum chloride (16.66 g, 125 mmol) in dichloromethane (100 mL) was added 1-acetyl-4-piperidinecarbonyl chloride (12.33 g, 65.0 mmol) at −10° C. Thioanisole (6.21 g, 50.0 mmol) was added dropwise at −10° C., the reaction mixture was stirred at room temperature for 1.5 hours. The reaction mixture was poured into ice water (80 g), the organic layer was separated and the aqueous layer was extracted with dichloromethane (40 mL) The combined organic layers were washed with 1N aqueous sodium hydroxide (2×40 mL), brine (40 mL), dried over anhydrous magnesium sulfate, filtered, and evaporated under reduced pressure. Ethyl acetate and diethyl ether was added to the residue, the resulting precipitate was collected by filtration, washed with diethyl ether, and dried under reduced pressure to afford the title compound (11.43 g, 41.2 mmol, 82%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348324B2
Source datasetuspto-grants-2008_03
ORD IDord-2cef58f7a40b40fdb9732e67786a1206
Source noteuspto-grants-2008_03