Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210719Generated: November 2, 2026

Epichlorohydrin → HCID 15670859, compound

https://huagongshe.com/reaction/2210719

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 numberUSRE035072
Source datasetuspto-grants-1995_10
ORD IDord-6625e060b47440e7a4a5d04603106c74
Source noteuspto-grants-1995_10