Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444691Generated: October 25, 2026

Ethyl trifluoroacetate → 1-(3,5-Dichloro-2-hydroxyphenyl)-2,2,2-trifluoroethanone

https://huagongshe.com/reaction/444691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant2,4-Dichloro-6-iodophenolHCID 4559010—
ReactantHCID 178461733HCID 178461733—
SolventTetrahydrofuranHCID 8028—
Product1-(3,5-Dichloro-2-hydroxyphenyl)-2,2,2-trifluoroethanoneHCID 5804115967.1%

Reaction Conditions

Temperature-35 °C

Reaction Steps

2,4-Dichloro-6-iodophenol (2.0 grams (g), 6.9 millimoles (mmol)) was dissolved in dry tetrahydrofuran (THF; 20 milliliters (mL)), cooled to −30 to −40° C., treated in portions with isopropyl magnesium chloride-lithium chloride complex (1.3 M in THF; 7.3 mmol) and stirred for 45 minutes (min) as the temperature was allowed to rise to 0° C. The mixture was cooled to −30° C., treated with 8 mL (10 mmol) of the Grignard reagent and stirred for 30 min at −30° C. Ethyl trifluoroacetate (2.4 mL, 2.8 g, 20 mmol) was added, and the mixture was stirred for 15 min at −30° C., warmed to 25° C. and stirred for 2 hours (h). The reaction was quenched by addition of saturated (satd) ammonium chloride (NH4C1; 10 mL), diluted with ethyl acetate (EtOAc; 50 mL) and washed with 1 M hydrochloric acid (HCl; 20 mL), satd sodium chloride (NaCl; 10 mL), dried over sodium sulfate (Na2SO4) and evaporated. The residue was purified by silica gel chromatography with 0-20% EtOAc/hexane to give the purified ketone (1.2 g): mp 50-52° C.; 1H NMR (400 MHz, CDCl3) δ 7.61 (d, J=2.4 Hz, 1H), 7.34 (d, J=2.4 Hz, 1H), 5.92 (s, 1H); EIMS m/z 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476194B2
Source datasetuspto-grants-2013_07
ORD IDord-c810a1216bcd4e22aeca6e737518006f
Source noteuspto-grants-2013_07