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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448325Generated: October 30, 2026

4-Isopropylaniline → HCID 58307336, compound

https://huagongshe.com/reaction/448325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IsopropylanilineHCID 7464—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
ReactantDimethyl 3-iodophthalateHCID 2326127—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 58307336HCID 5830733670%

Reaction Steps

A mixture of 3-iodophthalic acid dimethyl ester (1.0 g, 3.1 mmol), 4-isopropylaniline (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 0.70 g of the product at 85:15 hexanes-ethyl acetate, in 70% yield: 1H NMR (CDCl3) δ 1.25 (s, J=6.8 Hz, 6H), 2.90 (m, 1H), 3.86 (s, 3H), 3.88 (s, 3H), 7.01-7.13 (m, 3H), 7.27-7.34 (m, 4H), 8.07 (br, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481568B2
Source datasetuspto-grants-2013_07
ORD IDord-0b570fa84af549c59e1703f9ef84623d
Source noteuspto-grants-2013_07