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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053542Generated: November 2, 2026

Water → HCID 87088126, compound

https://huagongshe.com/reaction/1053542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantHypobromous acid, anhydride with propanoic acidHCID 11228909—
ReactantHCID 59539494HCID 59539494—
CatalystTetrabutylammonium ChlorideHCID 70681—
ProductHCID 87088126HCID 8708812690%

Reaction Steps

A mixture of (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaen-1-ol, (1.00 g, 3.47 mmol), tetrabutylammonium chloride (0.24 g, 0.87 mmol) and t-butyl □-bromo propionate (3.62 g, 17.3 mmol) was dissolved in toluene (36 mL) and placed under nitrogen. An aqueous solution of sodium hydroxide (50%, 8 mL) was added slowly under vigorous stirring and the resulting mixture was stirred at ambient temperature for twenty hours. Water was added and the mixture was extracted three times with ether. The combined organic extract was washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography on silica gel using 2% ethyl acetate in heptane as eluent. Concentration of the appropriate fractions afforded 1.40 g (90% yield) of the title compound as an oil. 1H-NMR (300 MHz, CDCl3): δ 0.95 (t, 3H), 1.41 (d, 3H), 1.48 (s, 9H), 1.48-1.66 (m, 4H), 2.05 (m, 4H), 2.83 (m, 8H), 3.35 (m, 1H), 3.55 (m, 1H), 3.79 (q, 1H), 5.32-5.44 (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394228B2
Source datasetuspto-grants-2016_07
ORD IDord-07caf6a8b2a14f6481c3773f66f89098
Source noteuspto-grants-2016_07