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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713844Generated: October 25, 2026

Diethyl Ether → Diarachidonyl Ketone

https://huagongshe.com/reaction/713844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium CarbonateHCID 11430—
ReactantDiarachidonyl MethanolHCID 58559615—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductDiarachidonyl KetoneHCID 58559565—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186325B2
Source datasetuspto-grants-2015_11
ORD IDord-4a0beae47fa4457f8f525168f743ea55
Source noteuspto-grants-2015_11