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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530929Generated: October 25, 2026

Dimethylformamide → Tert-butyl {4-[2-(benzyloxy)-2-oxoethyl]phenoxy}acetate

https://huagongshe.com/reaction/530929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantBenzyl 2-(4-hydroxyphenyl)acetateHCID 11107524—
SolventWaterHCID 962—
ProductTert-butyl {4-[2-(benzyloxy)-2-oxoethyl]phenoxy}acetateHCID 6835770498.3%

Reaction Steps

Potassium carbonate (1.38 g) and tert-butyl bromoacetate (1.07 g) were added to a dehydrated N,N-dimethylformamide (17 mL) solution of benzyl (4-hydroxyphenyl)acetate (1.21 g) at room temperature, followed by stirring for 1 hour. Thereafter, water was added to the reaction mixture on an ice bath, and extraction was performed with hexane:ethyl acetate=2:1. The resulting organic phase was washed with an aqueous saturated sodium chloride solution and dried with anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→8:2) to obtain the title compound (1.75 g) having the following physical property values.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353113B2
Source datasetuspto-grants-2016_05
ORD IDord-4bb030380e974bc88169e9b0d50458a6
Source noteuspto-grants-2016_05