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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210723Generated: November 2, 2026

Epichlorohydrin → HCID 15670859, compound

https://huagongshe.com/reaction/2210723

Reaction equation

Participants

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

Reaction Steps

To a mixture of epichlorohydrin (3.9 mL, 50 mmol) in EtOH (25 mL) and anhydrous NaHCO3 (4.2 g, 50 mmol), 1-piperonylpiperazine (11.0 g, 50 mmol) in EtOH (125 mL) was added dropwise 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% MeOH:CH2Cl2) 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-69f8d5e5705a4af0bff1a9ef97446dd5
Source noteuspto-grants-1995_10