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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476616Generated: October 30, 2026

Epichlorohydrin → HCID 15670859, compound

https://huagongshe.com/reaction/476616

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 numberUS04885300
Source datasetuspto-grants-1989_12
ORD IDord-4a0908fcb2394b3098fe65ceb5d50f4e
Source noteuspto-grants-1989_12