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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 354696Erstellt: 26. Oktober 2026

Toluene → Ethyl 2-(1-nonen-1-yl)-3,3-dimethylcyclopropanecarboxylate

https://huagongshe.com/reaction/354696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktEthyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylateHCID 566079—
EduktOctyltriphenylphosphonium bromideHCID 3084855—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktEthyl 2-(1-nonen-1-yl)-3,3-dimethylcyclopropanecarboxylateHCID 5418888157%

Reaktionsschritte

64.5 g of a 15% strength solution of butyl-lithium in n-hexane were added dropwise to a suspension of 68.3 g (0.15 mol) of n-octyl-triphenylphosphonium bromide in 300 ml of absolute tetrahydrofuran at 0°-5° C., with the exclusion of air. After one hour, 25.5 g (0.15 mol) of ethyl 2-formyl-3,3-dimethylcyclopropanecarboxylate were slowly added, and the mixture was further stirred for 18 hours at room temperature. The mixture was shaken after the addition of 400 ml of toluene and 300 ml of water, the water was separated off and the organic phase was washed once again with 200 ml of water. The toluene solution was then dried over sodium sulphate and the solvent was distilled off in vacuo. The residue was stirred with 300 ml of petroleum ether (40°-60° C.), the solution was filtered off from the undissolved triphenylphosphine oxide, and the filtrate was again concentrated by evaporation in vacuo. The residue was distilled in vacuo. 22.6 g (57% of theory) of ethyl 2-(1-nonen-1-yl)-3,3-dimethylcyclopropanecarboxylate with a boiling point of 90° C./0.01 mm Hg were thus obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04376786
Quelldatensatzuspto-grants-1983_03
ORD IDord-180eb195a3fc49f1b48ad354030375a7
Quellennotizuspto-grants-1983_03