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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351886Generated: November 1, 2026

Water → HCID 19844666, compound

https://huagongshe.com/reaction/2351886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 19844683HCID 19844683—
SolventBenzeneHCID 241—
ProductHCID 19844666HCID 19844666—

Reaction Steps

To a mixture containing 10.6 g of 1-[2-[1-(2,5-dimethylphenyl)-1-phenylpropoxy]ethyl]piperazine and 4.6 g of anhydrous, powdered potassium carbonate in 90 ml of anhydrous benzene, 3.6 g of allyl bromide dissolved in 10 ml of benzene are dropped while mild refluxing, then the reaction mixture is boiled for one additional hour. After cooling down, water is added to the mixture, the organic phase is separated, washed with water until neutral, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The anhydrous ethanolic solution of the evaporation residue is treated with an ethanolic fumaric acid solution. The solid precipitate is recrystallized from methanol to give the aimed dihydrogen fumarate, m.p. 202°-204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874765
Source datasetuspto-grants-1989_10
ORD IDord-aa3b11f26b6d4db58de04161297c096c
Source noteuspto-grants-1989_10