Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683505Generated: November 1, 2026

Hydrochloric Acid → N-(8-Amino-6-fluoro-5-methyl-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/1683505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantEthyl trifluoroacetateHCID 9794—
ReactantHCID 22449502HCID 22449502—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductN-(8-Amino-6-fluoro-5-methyl-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)-2,2,2-trifluoroacetamideHCID 22449445—

Reaction Conditions

Temperature20 °C

Reaction Steps

The compound obtained in (8) above (1.66 gm) was dissolved into a mixed solvent of 70 ml of ethanol and 10 ml of THF. To the solution were added 2 ml of triethylamine and 1.5 ml of ethyltrifluoroacetate, followed by stirring for 20 hours at 20° C. The reaction product was added to dilute aqueous solution of hydrochloric acid and extracted with chloroform. The extract was washed with water, saturated sodium bicarbonate and saturated brine in this order, and dried over anhydrous sodium sulfate. After removal of the solvent by evaporation, the residue was subjected to silica gel column chromatography using chloroform as an eluant to obtain fractions containing the target compound. The fractions were concentrated to obtain 1.79 gm of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637770
Source datasetuspto-grants-1997_06
ORD IDord-b47860b8ccba4136a0075eca40a49a22
Source noteuspto-grants-1997_06