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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286343Generated: October 31, 2026

N-(2,2,3,3-tetrafluoropropionyl)-2,6-dinitro-4-(trifluoromethyl)aniline → HCID 12874793, compound

https://huagongshe.com/reaction/2286343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2,2,3,3-tetrafluoropropionyl)-2,6-dinitro-4-(trifluoromethyl)anilineHCID 12874792—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 12874793HCID 12874793—

Reaction Steps

A mixture of N-(2,2,3,3-tetrafluoropropionyl)-2,6-dinitro-4-(trifluoromethyl)aniline (20 grams), 200 ml. of ethanol, and 1.5 grams of 5 percent palladium on carbon was hydrogenated to 137 lbs. TLC showed three streaks. The solution was left standing for 11/2 hours, after which the expected product streak predominated. The reaction mixture was hydrogenated further (8 more lbs) then left standing another 20 minutes. The reaction mixture was then filtered and evaporated, leaving 17.8 grams of an orange solid. It was dissolved in about 75 ml. of water and 2.1 grams of NaOH, filtered, and acidified with slow dropwise addition of about 10 ml. of acetic acid in about 50 ml. of water. At about pH 5-6, a glob of sticky dark material coagulated onto the stirrer and was removed. The acidification was continued, yielding a flocculant precipitate which was separated by filtration and air dried. It was purified by dissolving it in a small amount of 1 percent NaOH solution and reacidifying with dilute acetic acid, yielding the expected product as a pale yellow solid which on rapid heating melted sharply at about 100° C., resolidified, and melted again at 216°-219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04265901
Source datasetuspto-grants-1981_05
ORD IDord-cb613df38e6e42e1a80729393a083d61
Source noteuspto-grants-1981_05