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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 713844Erstellt: 24. Oktober 2026

Diethyl Ether → Diarachidonyl Ketone

https://huagongshe.com/de/reaction/713844

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktPotassium CarbonateHCID 11430—
EduktDiarachidonyl MethanolHCID 58559615—
EduktHCID 178418287HCID 178418287—
LösungsmittelDichloromethaneHCID 6344—
ProduktDiarachidonyl KetoneHCID 58559565—

Reaktionsschritte

To a mixture of diarachidonyl methanol (IV, 0.41 g, 0.71 mmol) and anhydrous potassium carbonate (0.05 g) in 10 mL of CH2Cl2 was added pyridinium chlorochromate (PCC, 0.50 g, 2.3 mmol). The resulting suspension was stirred at room temperature for 90 mins. Ether (50 mL) was then added into the mixture, and the resulting brown suspension was filtered through a pad of floresil (30 mL). The pad was further washed with ether (3×30 mL). The ether filtrate and washes were combined. Evaporation of the solvent gave 0.40 g of an oily residual as a crude product. The crude product was purified by column chromatography on silica gel (230-400 mesh, 10 mL) eluted with 0-3% ether in hexanes. This afforded 0.30 g (75%) of diarachidonyl ketone (V). 1H NMR (400 MHz, CDCl3) δ: 5.3-5.5 (16H, m, 8×CH═CH), 2.82 (12H, t, 6×C═C—CH2—C═C), 2.40 (4H, t, 2×CO—CH2), 2.08 (8H, m, 4× allylic CH2), 1.25-1.65 (20H, m), 0.90 (6H, t, 2×CH3) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09186325B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-4a0beae47fa4457f8f525168f743ea55
Quellennotizuspto-grants-2015_11