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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 2-Bromo-1-chloro-3-fluorobenzene | HCID 21938660 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2-Chloro-6-fluorophenyl)-P-tolyl-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115662B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-bb67b9ce8ff54b159ef57efb02cf925d |
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| Source note | uspto-grants-2006_10 |
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