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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259380Generated: October 25, 2026

Octane → 1-(2-Ethylhexyl)-3-cyano-6-methylpyrid-2-one

https://huagongshe.com/reaction/259380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctaneHCID 356—
Reactant2-MethoxyethanolHCID 8019—
Reactant3-Buten-2-one, 4-methoxy-HCID 94297—
Reactant2-cyano-N-(2-ethylhexyl)acetamideHCID 4590704—
SolventDichloromethaneHCID 6344—
Product1-(2-Ethylhexyl)-3-cyano-6-methylpyrid-2-oneHCID 2031218190%

Reaction Steps

N-(2-ethylhexyl) cyanoacetamide (60.4 g., 0.30 mole), 4-methoxy-3-butene-2-one (60.0 g., 0.60 mole), methylcello-solve (250 ml.) and 1,4-diazobicyclo [2.2.2.] octane (6.0 g.) are heated at reflux for 4 hours. Additional 4-methoxy-3-butene-2-one (30 g.) is added and reflux is continued for another 2 hours. The solvent is removed in vacuo to give an oil. The oil is dissolved in methylene chloride and extracted first with 2N--HCl (150 ml.) and then with water (2 × 250 ml.). The organic layer is dried over sodium sulfate, filtered and evaporated to dryness to give a 90% yield of crude product which is characterized by nmr and ir analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038065
Source datasetuspto-grants-1977_07
ORD IDord-d786c996b26840b6a7aeeb62ddc1c96d
Source noteuspto-grants-1977_07