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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463453Generated: October 26, 2026

Water → 4-(2-Chloro-1,1,2-trifluoroethoxy)-2,5-dichlorobenzenamine

https://huagongshe.com/reaction/463453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorotrifluoroethyleneHCID 6594—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Amino-2,5-dichlorophenol hydrochlorideHCID 13517288—
SolventDimethylformamideHCID 6228—
Product4-(2-Chloro-1,1,2-trifluoroethoxy)-2,5-dichlorobenzenamineHCID 1351729059%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 25 g (0.12 mole) of 4-amino-2,5-dichlorophenol hydrochloride in 200 ml dimethylformamide was placed in a 500 ml 3-necked round bottom flask, fitted with a mechanical stirrer, thermometer, reflux condenser and sparger, and 13.4 g (0.24 mole) of potassium hydroxide pellets ground to powder were added. The mixture was heated to 90° C. with stirring under a nitrogen blanket. Then 21 g (0.18 mole) chlorotrifluoroethylene was bubbled in, while stirring and heating at 90° to 100° C., in about 1/2 hour. Stirring was continued for 5 minutes, the mixture cooled in an ice water bath, 500 ml of water were added and the resulting mixture extracted with 250 ml methylene dichloride and then 100 ml methylene dichloride. The extracts were combined, washed with 250 ml water and the methylene dichloride removed in a rotary evaporator. The residue was distilled through a 1"×10" Vigreaux. The cut from 110° to 120° C. at 2 mm pressure was a light tan liquid. Weight 21 grams. Yield was 59 percent. NMR analysis verified structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518804
Source datasetuspto-grants-1985_05
ORD IDord-2a1053070b35474995a2c4f326db83c2
Source noteuspto-grants-1985_05