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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165793Generated: October 31, 2026

Methyl iodide → 1-Methyl-3-(4-chlorophenyl)piperazine dihydrochloride

https://huagongshe.com/reaction/1165793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium CarbonateHCID 10340—
Reactant2-(4-Chlorophenyl)piperazineHCID 3870273—
SolventWaterHCID 962—
Product1-Methyl-3-(4-chlorophenyl)piperazine dihydrochlorideHCID 1378744520.8%

Reaction Steps

A mixture of 10 g (0.051 mol) of 2-(4-chlorophenyl)piperazine (comparison product CP 1 of Table IV below; M.p=124° C.) 10.80 g (0.102 mol) of Na2CO3, 7.24 g (0.051 mol) of ICH3 and 100 ml of water is heated under reflux for 6 hours. It is cooled, extraction is carried out with CHCl3 and the chloroform phase is washed with water and dried over MgSO4. It is filtered, the filtrate is evaporated to dryness, the evaporation residue is taken up with CH3OH and the mixture is acidified with a solution of hydrochloric acid in ethanol. It is evaporated to dryness; recrystallization of the evaporation residue from a methanol/ethyl acetate mixture (1:1 v/v) gives 3 g (yield: 20.8%) of CRL 41 202. M.p.inst. =200° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04912110
Source datasetuspto-grants-1990_03
ORD IDord-0035001b7ab742b683aee3c2b2de8108
Source noteuspto-grants-1990_03