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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448356Generated: October 29, 2026

N,N-dimethyl-p-phenylenediamine → HCID 58307143, compound

https://huagongshe.com/reaction/448356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-dimethyl-p-phenylenediamineHCID 7472—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
ReactantDimethyl 3-iodophthalateHCID 2326127—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 58307143HCID 5830714371%

Reaction Steps

A mixture of 3-iodophthalic acid dimethyl ester (1.0 g, 3.1 mmol), N,N-dimethyl-1,4-phenylenediamine (0.42 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 0.73 g of the product at 70:30 hexanes-ethyl acetate, in 71% yield: 1H NMR (CDCl3) δ 2.95 (s, 6H), 3.86 (s, 3H), 3.88 (s, 3H), 6.71-6.76 (m, 2H), 6.88 (d, J=7.4 Hz, 1H), 7.00-7.09 (m, 3H), 7.20 (t, J=7.9 Hz, 1H), 8.10 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481568B2
Source datasetuspto-grants-2013_07
ORD IDord-ebbbdaf10d30433b9dd61d104db6fe0d
Source noteuspto-grants-2013_07