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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379682Generated: October 30, 2026

3-Methylbenzylpiperazine → HCID 18955924, compound

https://huagongshe.com/reaction/2379682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbenzylpiperazineHCID 79213—
ReactantHCID 18955928HCID 18955928—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 18955924HCID 1895592453%

Reaction Steps

The crude piperazine derivative from above (11.0 g, 56 mmole) was dissolved in 150 ml of toluene and added to 19.2 g (56 mmole) of 3-benzyloxy-4'-chlorobenzhydryl chloride (see U.S. Pat. No. 4,757,074) and heated to reflux for 40 hours. The reaction was cooled to room temperature, diluted to 600 ml with diethyl ether, and washed with 100 ml of 1.0M sodium hydroxide followed by three 200 ml portions of water and 100 ml of saturated sodium chloride. The product was dried over sodium sulfate and the solvent removed to give 27.0 g of crude product as a dark oil. The material was purified by chromatography on silica gel (Waters Prep 500) with 0.1% triethylamine in dichloromethane to give 14.7 g (53%) of 1-(3-benzyloxy-4'-chlorobenzhydryl)-4-(3-methylbenzyl)piperazine as a dark oil. A 5.0 g portion of the oil was dissolved in 300 ml of 2:1 ethanol:methanol and treated with an excess of ethanolic hydrochloric acid to produce the dihydrochloride salt of the product. Addition of 150 ml diethyl ether and cooling provided 1.74 g of the salt as white crystals, mp. 204°-208° C. Calc. for C32H33ClN2O 2HCl: C, 67.43; H, 6.19; N, 4.91; Cl, 18.66. Found: C, 67.15; H, 6.14; N, 4.87; Cl, 18.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364843
Source datasetuspto-grants-1994_11
ORD IDord-3dcbb7a367b048a9be220fe21a3efa4c
Source noteuspto-grants-1994_11