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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464794Generated: November 1, 2026

Potassium Carbonate → (E)-N-ethyl-N-(6-methoxy-6-methyl-2-hepten-4-ynyl)-5-formyl-2-furylmethylamine

https://huagongshe.com/reaction/1464794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhosphorus tribromideHCID 24614—
Reactant5-(Hydroxymethyl)furfuralHCID 237332—
Reactant(E)-N-ethyl-6-methoxy-6-methyl-2-hepten-4-ynylamine hydrochlorideHCID 19917137—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product(E)-N-ethyl-N-(6-methoxy-6-methyl-2-hepten-4-ynyl)-5-formyl-2-furylmethylamineHCID 1991704775.2%

Reaction Steps

0.36 g of 5-hydroxymethyl-2-furaldehyde was dissolved in 10 ml of ethyl ether, and under a nitrogen atmosphere, a ethyl ether solution (2 ml) of 0.25 g of phosphorus tribromide was added dropwise at 0° C. After the mixture was stirred at room temperature for 30 minutes, 0.70 g of potassium carbonate and a dimethylformamide solution (15 ml) of 0.62 g of (E)-N-ethyl-6-methoxy-6-methyl-2-hepten-4-ynylamine hydrochloride were added. The mixture was stirred overnight at room temperature, and then worked up in a customary manner. The product was purified by silica gel column chromatography [hexane/ethyl acetate=2/1] to give 0.62 g of (E)-N-ethyl-N-(6-methoxy-6-methyl-2-hepten-4-ynyl)-5-formyl-2-furylmethylamine as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306728
Source datasetuspto-grants-1994_04
ORD IDord-13ad9b3f24bd425aafdec96e8841e640
Source noteuspto-grants-1994_04