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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3764생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Carbonate IonHCID 19660—
반응물1,4-DioxaneHCID 31275—
반응물(Z,Z)-11,13-HexadecadienalHCID 6436739—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
용매WaterHCID 962—
생성물(12Z,14Z)-heptadeca-1,12,14-trieneHCID 6443230—

반응 단계

(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 The mixture was heated to reflux at 105°-110° with stirring while aliquots of 15 ul were withdrawn periodically and partitioned between 1 ml of H2O and 1 ml of hexane.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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04722839
출처 데이터셋uspto-grants-1988_02
ORD IDord-d08bf726ee614cf79e621b0c1f4b7772
출처 메모uspto-grants-1988_02