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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234864Generated: October 31, 2026

(R)-3-Benzyloxy-1-tetradecanol → (R)-3-(Benzyloxy)tetradecanoic acid

https://huagongshe.com/reaction/234864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-3-Benzyloxy-1-tetradecanolHCID 11723551—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product(R)-3-(Benzyloxy)tetradecanoic acidHCID 11110428—

Reaction Steps

Jones reagent was added in portions to a mixture of alcohol 46 (3.23 g, 10.1 mmol) in acetone (50 mL) at 0° C. until the alcohol was consumed. The mixture was partitioned between 0.1M HCl (100 mL) and ethyl acetate (400 mL), and the organic phases were washed with brine (100 mL), dried, and concentrated in vacuo. The product was purified by flash chromatography to give compound 47 as an oil (Rf 0.38, silica, 25% ethyl acetate in hexane, 2.09 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597573
Source datasetuspto-grants-1997_01
ORD IDord-88a2d1837eb348199a93bfcda4e0b082
Source noteuspto-grants-1997_01