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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359388Generated: October 29, 2026

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

https://huagongshe.com/reaction/359388

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 numberUS05001127
Source datasetuspto-grants-1991_03
ORD IDord-3c62edc2b0e34ab7a9f976b4f7ef618b
Source noteuspto-grants-1991_03