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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612443Generated: November 1, 2026

Potassium Carbonate → 1-(2-(6,11-Dihydrodibenzo[b,e]thiepin-11-ylidene)-1-ethyl)-4-piperidinecarboxylic acid ethyl ester hydrogen oxalate

https://huagongshe.com/reaction/612443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant11-(2-Bromoethylidene)-6,11-dihydrodibenzo[b,e]thiepineHCID 53962804—
CatalystSodium IodideHCID 5238—
SolventBenzeneHCID 241—
SolventDimethyl SulfoxideHCID 679—
Product1-(2-(6,11-Dihydrodibenzo[b,e]thiepin-11-ylidene)-1-ethyl)-4-piperidinecarboxylic acid ethyl ester hydrogen oxalateHCID 6994894772%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 11-(2-bromoethylidene)-6,11-dihydrodibenzo[b,e]thiepine (4.76 g, 0.015 mol, prepared similarly as described in Coll. Czech. Chem. Comm. 52, 1566, 1987) in dimethylsulfoxide (90 ml), potassium carbonate (3.1 g, 0.0225 mol), 4-piperidinecarboxylic acid ethyl ester (2.36 g, 0.015 mol) and sodium iodide (50 mg) were added and the mixture was stirred at 100° C. for 4 h. The reaction mixture was diluted with benzene (100 ml), the solid was filtered off and the filtrate was washed with water (4×60 ml). The benzene solution was dried (MgSO4) and the solvent removed in vacuo. The oily residue (6.34 g) was dissolved in acetone and treated with an ethanolic solution of oxalic acid. The resulting precipitate was filtered off and washed with a hot mixture of ethanol and acetone, affording 5.2 g (72%) of 1-(2-(6,11-dihydrodibenzo[b,e]thiepin-11-ylidene)-1-ethyl)-4-piperidinecarboxylic acid ethyl ester hydrogen oxalate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06004983
Source datasetuspto-grants-1999_12
ORD IDord-a01a8f87d24b4cfcbd7c568aee95928f
Source noteuspto-grants-1999_12