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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210717Generated: November 2, 2026

Epichlorohydrin → 4-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazine

https://huagongshe.com/reaction/2210717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantBenzhydrylpiperazineHCID 70048—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product4-(3-Chloro-2-hydroxypropyl)-1-diphenylmethylpiperazineHCID 10360175—

Reaction Steps

Diphenylmethylpiperazine (16.4 g, 0.065 mol) in ethanol (250 mL) was added dropwise to epichlorohydrin (5.1 mL, 0.065 mL) in ethanol (13 mL) with anhydrous NaHCO3 (0.065 mol, 5.46 g) at 0° C., over 45 min at room temperature under N2. After 17 h the NaHCO3 was removed by filtration via a sintered glass funnel and the ethanol removed from the filtrate in vacuo giving a white-yellow solid (21.5 g). This solid after triturating with Et2O (300 mL) gave a precipitate which was filtered and dried in vacuo to give the pure product (5.11 g, 22.8%) mp 114°-116° C. DCI/MS (M+1) 345. 400 MHz 1H NMR (CDCl3)δ:7.2-7.4 (m, 10H),4.2 (s,1H), 3.9 (m, 1H),3.55-3.7(m,2H),2.7(m,2H),2.45(m,8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE035072
Source datasetuspto-grants-1995_10
ORD IDord-9fde9d9f018047cba0dcc463f8915885
Source noteuspto-grants-1995_10