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HRID 26988作成日:2026年10月25日

Triethylamine → (E,E,E)-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol diisonicotinate

https://huagongshe.com/reaction/26988

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物(2E,6E)-2-[(3E)-4,8-Dimethylnona-3,7-dien-1-YL]-6-methylocta-2,6-diene-1,8-diolHCID 6373042—
反応物Isonicotinoyl chloride hydrochlorideHCID 12262826—
溶媒ChloroformHCID 6212—
生成物(E,E,E)-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol diisonicotinateHCID 86736498—

反応手順

To a solution of 1.0 g of (E,Z,E) and (E,E,E)-7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol in 30 ml of anhydrous chloroform was added 3.0 ml of triethylamine and then 2.0 g of isonicotinoyl chloride hydrochloride dropwise at room temperature. Stirring was continued for 3 hours. The reaction mixture was poured into ice-water, extracted with chloroform, washed with aqueous sodium hydrogencarbonate and water and dried over anhydrous sodium sulfate. The solvent was distilled off to give an oily substance, which was then purified by a column chromatography with silica gel (20 g) to afford 1.4 g of the end product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151357
出典データセットuspto-grants-1979_04
ORD IDord-1c0b5f3210f745a995389c63ca02bf59
出典メモuspto-grants-1979_04