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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658335Generated: October 29, 2026

Benzophenone → 3-tert-Butoxy-5-fluoroaniline

https://huagongshe.com/reaction/658335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium MethoxideHCID 10942334—
Reactant1-Bromo-3-tert-butoxy-5-fluorobenzeneHCID 56844292—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product3-tert-Butoxy-5-fluoroanilineHCID 66743914—

Reaction Conditions

Temperature80 °C

Reaction Steps

1-Bromo-3-tert-butoxy-5-fluorobenzene (56.1 g), benzophenone (50.9 g), NaOMe (50.5 g) and 2,2′-Bis-diphenylphosphanyl-[1,1′]binaphthalenyl (17.5 g) are dissolved in toluene (500 ml). The reaction mixture is flushed with argon, Pd2(dba)3 (5.4 g) is added and the reaction mixture is heated to 80° C. for 40 hours. The reaction mixture is quenched with water. The organics are separated, dried over MgSO4, filtered and the solvent removed in vacuo. The intermediate is obtained by flash column chromatography (silica, eluent dichloromethane). The resulting product is then dissolved in MeOH (1 L). NaOAc (46.1 g), hydroxylamine hydrochloride (29.1 g) are added and the reaction mixture is stirred at room temperature for 2.5 hours. The reaction mixture is quenched with 0.1M NaOH, extracted into DCM (2×), dried over MgSO4, filtered and the solvent removed in vacuo to give the title compound. 1H nmr (CDCl3, 400 MHz); 6.20 (m, 3H), 3.75 (br s, 2H), 1.4 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076489B2
Source datasetuspto-grants-2011_12
ORD IDord-b39c6c4777ea4c5a9cb839923abbe3c1
Source noteuspto-grants-2011_12