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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448355Generated: October 26, 2026

Cesium carbonate → 3-(2-Phenoxyphenylamino)phthalic acid dimethyl ester

https://huagongshe.com/reaction/448355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBenzenamine, 2-phenoxy-HCID 75899—
ReactantBinap, (A+-)-HCID 634876—
ReactantDimethyl 3-iodophthalateHCID 2326127—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product3-(2-Phenoxyphenylamino)phthalic acid dimethyl esterHCID 5830726373%

Reaction Steps

A mixture of 3-iodophthalic acid dimethyl ester (1.0 g, 3.1 mmol), 2-phenoxyaniline (0.57 g, 3.1 mmol), Pd2(dba)3 (0.13 g, 0.14 mmol), rac-BINAP (0.058 g, 0.093 mmol), and cesium carbonate (1.4 g, 4.3 mmol), in 6 mL toluene was heated to reflux under nitrogen for 24 hours. The reaction mixture was cooled, diluted with CH2Cl2 (10 mL), and filtered through Celite, and the filter was washed with additional CH2Cl2 (30 mL). The filtrate was evaporated, and the residue was chromatographed using a hexanes-ethyl acetate gradient, eluting 0.86 g of the product at 80:20 hexanes-ethyl acetate, in 73% yield: 1H NMR (CDCl3) δ 3.75 (s, 3H), 3.86 (s, 3H), 6.93-7.03 (m, 4H), 7.06-7.12 (m, 2H), 7.17 (dd, J=7.3 Hz, J=1.0 Hz, 1H), 7.29-7.38 (m, 4H), 7.46 (d, J=8.4 Hz, 1H), 7.89 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481568B2
Source datasetuspto-grants-2013_07
ORD IDord-6473256ac8d046dcad2dccea91f9a60d
Source noteuspto-grants-2013_07