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HRID 354696作成日:2026年10月27日

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

https://huagongshe.com/reaction/354696

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Ethyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylateHCID 566079—
反応物Octyltriphenylphosphonium bromideHCID 3084855—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Ethyl 2-(1-nonen-1-yl)-3,3-dimethylcyclopropanecarboxylateHCID 5418888157%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04376786
出典データセットuspto-grants-1983_03
ORD IDord-180eb195a3fc49f1b48ad354030375a7
出典メモuspto-grants-1983_03