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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359390Generated: November 1, 2026

Epichlorohydrin → HCID 15670859, compound

https://huagongshe.com/reaction/359390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactant1-PiperonylpiperazineHCID 94426—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
ProductHCID 15670859HCID 1567085926.4%

Reaction Steps

1-Piperonylpiperazine (11.0 g, 50 mmol) in EtOH (125 mL) was added dropwise to epichlorohydrin (3.9 mL, 50 mmol) in EtOH (25 mL) and NaHCO3 (4.2 g, 50 mmol) over 45 min at 0° C., under nitrogen. After 16 h and removal of the EtOH in vacuo, the crude material was passed through silica gel (vacuum, 5% methanol: methylene chloride) to give pure product (3.85 g, 26.4%) as an amber oil. DCI/MS (M+1) 313. 400 MHz 1H NMR (CDCl3) δ: 7.25 (s, 1H), 6.7-6.8 (m, 2H), 5.9 (s, 2H), 4.6 (m, 1H), 3.9 (m, 1H), 3.5 (m, 2H), 3.4 (s, 2H), 2.4-2.7 (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001127
Source datasetuspto-grants-1991_03
ORD IDord-6d578487694944348db60cff144d44d5
Source noteuspto-grants-1991_03