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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919766Generated: November 3, 2026

5-Hydroxy-2-pentanone → 5-(Benzyloxy)pentan-2-one

https://huagongshe.com/reaction/1919766

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Hydroxy-2-pentanoneHCID 14066—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product5-(Benzyloxy)pentan-2-oneHCID 28126865%

Reaction Steps

Benzyl trichloroacetimidate (1.85 g) was added to a mixed solution of 5-hydroxy-2-pentanone (500 mg, 4.89 mmol) in dichloromethane (20 mL) in an argon atmosphere at room temperature, and then trifluoromethanesulfonic acid (87 μL) was added in an ice bath. The mixture was returned to room temperature and stirred overnight. After completion of the reaction, a saturated sodium bicarbonate solution was added to the reaction solution in an ace bath, and the pH was adjusted to 8. After extraction with chloroform-water, the organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to obtain 610 mg of the title compound (yield: 65%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168666B2
Source datasetuspto-grants-2012_05
ORD IDord-45f2d1c6054c457da73601f9485ec5b1
Source noteuspto-grants-2012_05