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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359391Generated: October 30, 2026

Epichlorohydrin → HCID 70046861, compound

https://huagongshe.com/reaction/359391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantNorchlorcyclizineHCID 9340—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 70046861HCID 7004686126.3%

Reaction Steps

4-Chlorobenzhydrylpiperazine (14.34 g, 50 mmol) in EtOH (150 mL) was added to epichlorohydrin (3.92 mL, 50 mmol) in ethanol (25 mL) and NaHCO3 (4.2 g, 50 mmol) over 45 min at 0° C. under nitrogen. After 20 h, the EtOH was removed in vacuo and the residue eluted through silica gel using 50% methanol: methylene chloride to give the pure product (3.40 g, 18.3%) as a white solid, mp 72°-74° C. DCI/MS (M+1) 379. 400 MHz 1H NMR (CDCl3) δ: 7.5-7.35 (m, 9H), 4.2 (s, 1H), 3.65 (m, 2H), 2.9 (m, 2H), 2.7-2.6 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001127
Source datasetuspto-grants-1991_03
ORD IDord-b09c010896a84577bb8b6c70b818c49a
Source noteuspto-grants-1991_03