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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509604Generated: October 29, 2026

Hydrochloric Acid → HCID 67967980, compound

https://huagongshe.com/reaction/509604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4-(trifluoromethoxy)anilineHCID 2734084—
ReactantTrimethylaluminumHCID 16682925—
ReactantMethyl 5-(2,2,2-trifluoroethoxy)pyridine-2-carboxylateHCID 57475873—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 67967980HCID 67967980—

Reaction Conditions

Temperature85 °C

Reaction Steps

2-Chloro-4-trifluoromethoxy-phenylamine (2.0 g, 9.29 mmol) in toluene (50 mL) was added to trimethylaluminum (2.0 M 4.65 mL) then 5-(2,2,2-Trifluoro-ethoxy)-pyridine-2-carboxylic acid methyl ester 3 (1.1 g, 4.65 mol) was added and the mixture was heated to 80-90° C. for 2 h. The reaction was cooled down and 1N HCl solution (10 mL) was added to be acidic. Dichloromethane (100 mL) was then added and the organic phase was further washed with water (100 mL) and dried over sodium sulfate. The solvent was removed and the residue was mixed with ether (50 mL) and stirred for 0.5 h. The solid was filtered and dried to give 5-(2,2,2-Trifluoro-ethoxy)-pyridine-2-carboxylic acid (2-chloro-phenyl)-amide 4 as a solid. Yield: 1.0 g, 71%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096587B2
Source datasetuspto-grants-2015_08
ORD IDord-746f7f786c024f4c9c14cdf73f04489c
Source noteuspto-grants-2015_08