戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 128779作成日:2026年10月25日

18-Crown-6 → 1-(2-Methoxyethenyl)-4-(octyloxy)benzene

https://huagongshe.com/reaction/128779

反応式

関与物質

役割名称HCID仕込み量
反応物18-Crown-6HCID 28557—
反応物p-(Octyloxy)benzaldehydeHCID 90358—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-(2-Methoxyethenyl)-4-(octyloxy)benzeneHCID 53775512—

反応手順

Potassium t-butoxide (1.9 g) is added to a slurry of methoxymethyl triphenylphosphonium chloride (6.17 g) and 18-Crown-6 (100 mg) in dry THF (40 ml). The mixture is stirred for 5 min, cooled to 15°, and a solution of 4-octyloxybenzaldehyde (3.52 g) in THF (5 ml) is added dropwise. The reaction mixture is stirred at room temperature for 20 min, diluted with 250 ml hexane, and the resulting mixture filtered through a pad of diatomaceous earth. Evaporation of the filtrate leaves crude 1-(2-methoxyethenyl)-4-(octyloxy)benzene as a mixture of cis and trans isomers, containing about 15 mol % triphenylphosphine oxide. The crude material may be used as is, or may be chromatographed with 1:1 hexanedichloromethane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464865
出典データセットuspto-grants-1995_11
ORD IDord-342bcfb170dd446095d890ba2b2078d3
出典メモuspto-grants-1995_11