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Volumn , Issue 4, 2007, Pages 543-546

Cyanation of aryl chlorides with potassium hexacyanoferrate(II) catalyzed by cyclopalladated ferrocenylimine tricyclohexylphosphine complexes

(4) Cheng, Yi Nan a Duan, Zheng a Li, Ting a Wu, Yangjie a

a ZHENGZHOU UNIVERSITY (China)

Author keywords

Aryl chloride; Catalysis; Coupling; Cyanation; Cyclopalladium

Indexed keywords

4 CHLOROTOLUENE; ARYL CHLORIDE DERIVATIVE; CHLORINE DERIVATIVE; FERROCENYLIMINE TRICYCLOHEXYLPHOSPHINE COMPLEX; FERROCYANIDE; PALLADIUM COMPLEX; PHOSPHINE DERIVATIVE; POTASSIUM; TOLUENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYANATION; OXIDATION;

EID: 33947235315 PISSN: 09365214 EISSN: None Source Type: Journal
DOI: 10.1055/s-2007-970741 Document Type: Article

Times cited : (37)

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- General Procedure. A reaction vessel was charged with 1 mmol Na2CO3, 0.22 mmol K4[Fe(CN)6] ·3H2O and 2% mol catalyst 2a. The vessel was then evacuated and backfilled with N2 four times. Then, 1 mmol aryl chloride in 1 mL NMP was added to the vessel. The mixture was heated at 140°C for 16-24 h. The suspension was cooled down to r.t, diluted with 5 mL CH2Cl2 and washed with 5 mL H2O. The aqueous layer was extracted twice with CH2Cl2 (3 mL) and the combined organic layers were dried over MgSO4. After evaporation of the solvents the residue was subjected to TLC (hexane-EtOAc, All prepared compounds were known and identified by 1H NMR, 13C NMR and MS. Selected Data. Compound 4c: 1H NMR (400 MHz, CDCl3, δ, 2.53 (s, 6 H, 7.11 (d, J, 7.7 Hz, 2 H, 7.34 dd, J
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