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HRID 256000作成日:2026年10月26日

1-Iodohexane → 1-Methoxy-3-(1-octynyl)benzene

https://huagongshe.com/reaction/256000

反応式

関与物質

役割名称HCID仕込み量
反応物1-IodohexaneHCID 12527—
反応物1-Ethynyl-3-methoxybenzeneHCID 640753—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物1-Methoxy-3-(1-octynyl)benzeneHCID 11264406—

反応条件

温度-70 °C

反応手順

3-Methoxyphenylacetylene [5.00 g, 0.032M, prepared by the method of E. Negishi et al, J. Org. Chem. 45 2526-8, (1980)] was dissolved in dry tetrahydrofuran (15 ml), cooled to -70° C. under nitrogen, and n-butyl lithium, 1.6M in hexane, (24.40 ml, 0.038M), added dropwise. After stirring for 0.5 h, iodohexane (8.00 g, 0.038M), dissolved in dry tetrahydrofuran, (15 ml) was added dropwise. The rection was warmed slowly to room temperature, refluxed overnight, then cooled. The solution was then quenched with water, acidified with dilute hydrochloric acid and extracted with diethyl ether (twice). The organic phases were combined, washed with water and dried, (MgSO4). Evaporation in vacuo affored 7.71 g of product as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04699995
出典データセットuspto-grants-1987_10
ORD IDord-b406641224384b73a1452fc6b9686c3f
出典メモuspto-grants-1987_10