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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341359Generated: October 25, 2026

Aniline → 2,3-difluoro-N-phenylaniline

https://huagongshe.com/reaction/341359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantBinap, (A+-)-HCID 634876—
Reactant1-Bromo-2,3-difluorobenzeneHCID 2733260—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product2,3-difluoro-N-phenylanilineHCID 6691112396.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1-bromo-2,3-difluorobenzene (0.232 mL, 2.073 mmol), aniline (0.208 mL, 2.280 mmol), Pd2(dba)3 (95 mg, 0.104 mmol), BINAP (194 mg, 0.311 mmol), sodium tert-butoxide (299 mg, 3.11 mmol), and toluene (3 mL) in a sealed vessel under argon was heated in an oil bath at 110° C. overnight. The reaction mixture was filtered through a plug of celite. The filtrate was concentrated and the residue was purified by silica gel column chromatography to give the title compound as a light brown oil (411 mg). LCMS m/z=206.1 [M+H]+; 1H NMR (400 MHz, Methanol-d4) δ ppm 6.53-6.64 (m, 1H), 6.80-6.88 (m, 2H), 6.88-6.95 (m, 1H), 6.95-7.03 (m, 2H), 7.11-7.19 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895776B2
Source datasetuspto-grants-2014_11
ORD IDord-2a9324ecdf414c34b3a9588ddf9af039
Source noteuspto-grants-2014_11