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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396881Generated: October 30, 2026

Potassium Carbonate → 1-(2-(2,3,4,5-Tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine

https://huagongshe.com/reaction/2396881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2,3,4,5-Tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl bromideHCID 18986519—
Reactant4-(3,4-Dimethoxyphenyl)piperidine hydrochlorideHCID 18986577—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-(2-(2,3,4,5-Tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidineHCID 18986523—

Reaction Steps

3.6 g of 2-(2,3,4,5-tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl bromide [obtainable starting from 2,3,4,5-tetrahydro-7-cyano-1-benzoexpin-5-one [sic] by reaction with triphenylethylphosphinium bromide, subsequent bromination of the product in the allyl position and reduction of the isolated double bond with diisobutyl-aluminiumhydride (DIBAH)], 1 equivalent of 4-(3,4-dimethoxyphenyl)piperidine hydrochloride, 3.8 g of K2CO3 and 2.1 g of KI are dissolved in 120 ml of ethyl methyl ketone and the mixture is boiled for 3 hours. Customary working up gives 1-(2-(2,3,4,5-tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05495022
Source datasetuspto-grants-1996_02
ORD IDord-af3eb4b01e1c4d9da7abb7616e6fe4d6
Source noteuspto-grants-1996_02