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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280987Generated: October 26, 2026

Diethyl Ether → Bis(linoleyl) ketone

https://huagongshe.com/reaction/2280987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium CarbonateHCID 10340—
ReactantDlin-MeOHHCID 44468963—
ReactantHCID 178418299HCID 178418299—
SolventDichloromethaneHCID 6344—
ProductBis(linoleyl) ketoneHCID 59544992—

Reaction Steps

To a mixture of dilinoleyl methanol (2.0 g, 3.8 mmol) and anhydrous sodium carbonate (0.2 g) in 100 mL of CH2Cl2 was added pydimium chlorochromate (PCC, 2.0 g, 9.5 mmol). The resulting suspension was stirred at room temperature for 60 min. Ether (300 mL) was then added into the mixture, and the resulting brown suspension was filtered through a pad of silica gel (300 mL). The silica gel pad was further washed with ether (3×200 mL). The ether filtrate and washes were combined. Evaporation of the solvent gave 3.0 g of an oily residual as a crude product. The crude product was purified by column chromatography on silica gel (230-400 mesh, 250 mL) eluted with 0-3% ether in hexanes. This gave 1.8 g (90%) of dilinoleyl ketone (V). 1H NMR (400 MHz, CDCl3) δ: 5.25-5.45 (8H, m, 4×CH═CH), 2.78 (4H, t, 2×C═C—CH2-C═C), 2.39 (4H, t, 2×COCH2), 2.05 (8H, q, 4×allylic CH2), 1.45-1.7 (4H, m), 1.2-1.45 (32H, m), 0.90 (6H, t, 2×CH3) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139554B2
Source datasetuspto-grants-2015_09
ORD IDord-6ae40e1f8ab3474f808ab853ebbd22fc
Source noteuspto-grants-2015_09