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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613357Generated: October 30, 2026

Ethyl Acetate → 3-(Benzyloxy)propanoic acid

https://huagongshe.com/reaction/613357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Benzyloxy-1-propanolHCID 347971—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product3-(Benzyloxy)propanoic acidHCID 15608813—

Reaction Steps

To 3-benzyloxy-1-propanol (1.66 g) dissolved in acetone (10 ml) was added 2N Jones reagent (10 ml) while cooling on ice, and the mixture was stirred for 4 hours at room temperature. Ethyl acetate was added, and the resultant mixture was washed with water. The organic layer was extracted with a sat. aq. K2CO3, and the aqueous layer was washed with ethyl acetate. The washed material was acidified with dilute HCl, again extracted with ethyl acetate, then washed with saturated brine. Drying over anhydrous magnesium sulfate and concentrating under reduced pressure yielded 1.27 g of 3-benzyloxypropionic acid as a colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008224
Source datasetuspto-grants-1999_12
ORD IDord-f91d08302f4b467885812208feee33b0
Source noteuspto-grants-1999_12