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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531111Generated: October 30, 2026

Potassium Carbonate → HCID 11123863, compound

https://huagongshe.com/reaction/1531111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
ReactantN,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
Reactant(4-Benzyloxy-phenylsulfonyl)-acetic acid ethyl esterHCID 10947619—
SolventAcetoneHCID 180—
ProductHCID 11123863HCID 11123863—

Reaction Steps

To a stirred solution of bis-(2-chloro-ethyl)-benzyl amine hydrochloride (6.6 g, 24.7 mmol), 18-Crown-6 (500 mg), and anhydrous K2CO3 (30 gm, excess) in dry acetone (250 ml), (4-benzyloxy-phenylsulfonyl)-acetic acid ethyl ester (8.01 gm, 24 mmol) was added in a round bottom flask and the reaction mixture was heated at reflux for 16 hours with good stirring. At the end, the reaction mixture was allowed to cool and the potassium salts were filtered off and the reaction mixture was concentrated. The residue was extracted with chloroform and washed with H2O. The organic layer was further washed well with water, dried over MgSO4, filtered and concentrated. The dark brown reaction mixture was purified by silica gel coumn chromatography by eluting it with 30% ethylacetate: hexane and the product 4-(4-Benzyloxy-benzenesulfonyl)-1-benzyl-piperidine-4-carboxylic acid ethyl ester was isolated as Brown oil. Yield: 6.5 g, 55%; MS: 494 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197791B1
Source datasetuspto-grants-2001_03
ORD IDord-84037ac7da0d4c2a8085d211d537c736
Source noteuspto-grants-2001_03