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HRID 370583作成日:2026年10月25日

Potassium Carbonate → (12Z,14Z)-heptadeca-1,12,14-triene

https://huagongshe.com/reaction/370583

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1,4-DioxaneHCID 31275—
反応物(Z,Z)-11,13-HexadecadienalHCID 6436739—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒WaterHCID 962—
生成物(12Z,14Z)-heptadeca-1,12,14-trieneHCID 6443230—

反応手順

(Z,Z)-1,12,14-heptadecatriene (TRIENE) was synthesized conveniently from Wittig Salt and aldehyde in aqueous dioxide-potassium carbonate heterogeneous medium (Lechat 1982). A mixture of 3.57 g (0.01 mol) of methyl triphenylphosphonium bromide (Alfa Inorganics), 1.7 g (0.14 mol) of potassium carbonate, 10 ml of 1,4-dioxane, 0.15 ml of water and 2.36 g (0.01 mol) of (Z,Z)-11,13-hexadecadienal (AL. Albany International) was prepared in a 100 ml round bottomed flask equipped with a magnetic stirrer, thermometer and reflux condenser. The mixture was heated to reflux at 105-110° with stirring while aliquots of 15 ul were withdrawn periodically and partitioned between 1 ml of H2O and 1 ml of hexane. Analysis by gas-liquid chromatography, showed 66,70 and 99% triolefin and 30%, 26% and 1% starting aldehyde at 1.1 and 2.2 and 17 hr, respectively. More potassium carbonate (1.7 g) was added at 212 hr to drive the reaction to completion. The reaction mixture was cooled and extracted 3 times with 25 ml of hexane, then the organic layer was extracted with water, dried and the solvent removed to leave 1.8 g of yellow oil and a few crystals of triphenylphosphine oxide. The oil was taken up in hexane and passed through a 1×45 cm column of silica gel (60-200 mesh, Baker) with hexane, to yield 1.7 g (73% yield) of clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04527000
出典データセットuspto-grants-1985_07
ORD IDord-2d9638eea79541e79ef33535609ad0ef
出典メモuspto-grants-1985_07