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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242255Generated: October 26, 2026

Hydrochloric Acid → (2-Chloro-6-fluorophenyl)-P-tolyl-amine

https://huagongshe.com/reaction/1242255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-ToluidineHCID 7813—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Bromo-1-chloro-3-fluorobenzeneHCID 21938660—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(2-Chloro-6-fluorophenyl)-P-tolyl-amineHCID 21100364—

Reaction Steps

A mixture of 146.1 g (1.36 mol) of p-toluidine, 12.6 g (0.02 mol) of (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl, 261.9 g (2.73 mol) of sodium t-butoxide, 314.1 g (1.50 mol) of 2-bromo-3-fluoro-chlorobenzene and 6.3 g (0.0069 mol) of tris(dibenzylideneacetone)dipalladium(0) in 3000 ml of toluene is heated to 110° over 30 minutes and stirred an additional 4 hours at this temperature. The mixture is cooled to room temperature and a solution of 680 ml 37% hydrochloric acid and 680 ml of water is added over 15 minutes. The mixture is stirred for 20 minutes and filtered through a pad of Celite. The layers are separated and the organic phase is washed twice with 680 ml of water and once with a solution of 225 g of sodium chloride in 680 ml of water. The solvents are evaporated under reduced pressure to give N-(2′-chloro-6′-fluorophenyl)-4-methylaniline as an oil, b.p. 129–131°/0.5 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115662B2
Source datasetuspto-grants-2006_10
ORD IDord-bb67b9ce8ff54b159ef57efb02cf925d
Source noteuspto-grants-2006_10