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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037796Generated: October 31, 2026

Triethylamine → 4-Acetyl-N-(2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1037796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-N-(2,2,2-trifluoroethyl)acetamideHCID 24705143—
Reactant4-Acetyl-1-naphthalenecarbonyl chlorideHCID 86649801—
Solvent1,2-DichloroethaneHCID 11—
Product4-Acetyl-N-(2-oxo-2-((2,2,2-trifluoroethyl)amino)ethyl)-1-naphthalenecarboxamideHCID 6686519175%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-amino-N-(2,2,2-trifluoroethyl)acetamide (21.90 g, 0.14 mol) in 1,2-dichloroethane (80 mL) was added dropwise over 15 min to a solution of the product of Example 7, Step A (32.50 g, 0.14 mol) in 1,2-dichloroethane (160 mL) at a temperature of 25 to 30° C. The resulting mixture was further stirred for 10 min at 25° C. A solution of triethylamine (14.20 g, 0.14 mol) in 1,2-dichloroethane (80 mL) was then added dropwise over 44 min at 25° C., and the mixture was stirred further for 20 min at 25° C. The solvent was removed under reduced pressure, and the residue was dissolved in hot acetonitrile (50 mL). The mixture was then cooled to 25° C., and water (40 mL) was added dropwise. The mixture was further cooled to 0° C. and filtered. The isolated solid was washed with water (100 mL) and dried overnight in a vacuum oven (approximately 16-33 kPa at 50° C.) to provide the title product as an off-white solid (37 g, 75% yield) melting at 169-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546618B2
Source datasetuspto-grants-2013_10
ORD IDord-f1e41d41f8d643aea9a2e03aaa85f42a
Source noteuspto-grants-2013_10