Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662589Generated: October 30, 2026

Ethyl Acetate → 3-(Trifluoromethoxy)anisole

https://huagongshe.com/reaction/1662589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Trifluoromethoxy)phenolHCID 2733261—
ReactantHCID 178477804HCID 178477804—
SolventDimethylformamideHCID 6228—
Product3-(Trifluoromethoxy)anisoleHCID 2777188128.4%

Reaction Steps

To a suspension of 20.0 g of 3-(trifluoromethoxy)phenol and 23.3 g of K2CO3 (anhydrous) in DMF (100 ml) was added 23.9 g of iodine methane under ice cooling, then the reaction mixture was warmed to room temperature, and was stirred at room temperature for 13 hours. To the reaction solution was added EtOAc (100 ml) and purified water (150 ml), and the resulting mixture was stirred for 30 minutes. After liquid separation, the aqueous layer was extracted with EtOAc (50 ml×2), the combined organic layer was washed with purified water (100 ml×3) and with saturated brine (50 ml) and dried overover MgSO4, then, the drying agent was separated by filtration, and the solvent was removed under reduced pressure to obtain 27.7 g of the title compound (crude form, yellow oil). The present compound was used in the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-d83b2692812547bfbbce45e530adebb8
Source noteuspto-grants-2011_10