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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36765Generated: October 28, 2026

Toluene → N-(2,6-Diisopropylphenyl)-2-[2-(4-phenylpiperazinyl)ethylsulfonyl]acetamide

https://huagongshe.com/reaction/36765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1-PhenylpiperazineHCID 7096—
ReactantN-(2,6-diisopropylphenyl)-2(2-chloroethylsulfonyl)acetamideHCID 19937765—
SolventEthyl AcetateHCID 8857—
ProductN-(2,6-Diisopropylphenyl)-2-[2-(4-phenylpiperazinyl)ethylsulfonyl]acetamideHCID 1993776870.7%

Reaction Steps

A mixture of 3.46 g of N-(2,6-diisopropylphenyl)-2(2-chloroethylsulfonyl)acetamide synthesized in (1) above, 1.62 g of N-phenylpiperazine, and 50 ml of toluene was heated under reflux for 4 hours. To the reaction mixture was added 100 ml of ethyl acetate, and the mixture was washed successively with a sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to column chromatography using a mixture of ethyl acetate and hexane at a ratio varying from 1:1 to 1:0 as a developing solvent. The solvent was evaporated, and the residue was dissolved in ethyl acetate and crystallized from a 4N hydrochloric acid solution in ethyl acetate to obtain 3.33 g of the title compound as white powder (m.p.=197.0°-200.0° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416212
Source datasetuspto-grants-1995_05
ORD IDord-2c01800daad5483f8931d0b7feb74107
Source noteuspto-grants-1995_05