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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476614Generated: October 31, 2026

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

https://huagongshe.com/reaction/476614

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 numberUS04885300
Source datasetuspto-grants-1989_12
ORD IDord-9afb6c93b8df40d28722c806b8ca897b
Source noteuspto-grants-1989_12