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HRID 3764作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/3764

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Carbonate IonHCID 19660—
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 dioxidepotassium 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 The mixture was heated to reflux at 105°-110° with stirring while aliquots of 15 ul were withdrawn periodically and partitioned between 1 ml of H2O and 1 ml of hexane.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US04722839
出典データセットuspto-grants-1988_02
ORD IDord-d08bf726ee614cf79e621b0c1f4b7772
出典メモuspto-grants-1988_02