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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476615Generated: October 31, 2026

Epichlorohydrin → HCID 11777838, compound

https://huagongshe.com/reaction/476615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactant1-BenzylpiperazineHCID 75994—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 11777838HCID 1177783875.3%

Reaction Steps

1-Benzylpiperazine (8.66 mL, 50 mmol) in EtOH (100 mL) was added dropwise to epichlorohydrin (3.92 mL, 50 mmol) in EtOH (25 mL) with NaHCO3 (4.2 g, 50 mmol) over 30 min at 0° C. under nitrogen. After 16 h the EtOH was removed in vacuo and the crude product eluted through silica gel (5% methanol: methylene chloride) to give pure product (10.12 g, 75.3%) as an amber oil. DCI/MS (M+1) 269. 400 MHz 1H NMR (CDCl3) δ: 7.3 (m, 5H), 4.95 (m, 1H), 4.5 & 4.6 (m, 2H), 3.95 (m, 1H), 3.6 (m, 2H), 3.5 (s, 2H), 2.7 (m, 4H), 2.4 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885300
Source datasetuspto-grants-1989_12
ORD IDord-30e9dde06a334f5a9ebacd0be9cbeb46
Source noteuspto-grants-1989_12