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75358-90-6

75358-90-6 Structure

75358-90-6 Structure
IdentificationBack Directory
[Name]

ETHYL 2-CYANOPYRIDINE-3-CARBOXYLATE
[CAS]

75358-90-6
[Synonyms]

ethyl 2-cyanonicotinate
Ethyl 2-cyanonicotinate 97+%
2-Cyano-nicotinic acid ethyl ester
ETHYL 2-CYANOPYRIDINE-3-CARBOXYLATE
Ethyl 2-cyanopyridine-3-carboxylate 97%
3-(Ethoxycarbonyl)-2-pyridinecarbonitrile
2-Cyanopyridine-3-carboxylic acid ethyl ester
2-cyano-3-pyridinecarboxylic acid ethyl ester
3-Pyridinecarboxylic acid, 2-cyano-, ethyl ester
[Molecular Formula]

C9H8N2O2
[MDL Number]

MFCD07368152
[MOL File]

75358-90-6.mol
[Molecular Weight]

176.17
Chemical PropertiesBack Directory
[Melting point ]

35-40°C
[Boiling point ]

185-195 °C(Press: 12 Torr)
[density ]

1.21
[storage temp. ]

2-8°C
[form ]

solid
[pka]

-2.25±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

36/37/39
[WGK Germany ]

3
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 2-CYANOPYRIDINE-3-CARBOXYLATE(75358-90-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

ZINC CYANIDE

557-21-1

Ethyl 2-chloronicotinate

1452-94-4

ETHYL 2-CYANOPYRIDINE-3-CARBOXYLATE

75358-90-6

To a solution of ethyl 2-chloropyridine-3-carboxylate (15.0 g, 81 mmol) in anhydrous N,N-dimethylacetamide (75 mL) was added zinc cyanide (5.71 g, 48.6 mmol), tris(dibenzylideneacetone)dipalladium (742 mg, 0.81 mmol), zinc powder (636 mg, 9.72 mmol), and 1,1'-bis(diphenylphosphinyl ) ferrocene (898 mg, 1.62 mmol). The reaction mixture was heated and stirred at 120 °C for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and then partitioned between water (300 mL) and ether (150 mL). The organic and aqueous phases were separated by Celite filtration of the mixture. The aqueous phase was further extracted with ether (2 x 100 mL), all ether layers were combined, washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give ethyl 2-cyanonicotinate (14.26 g, 100% yield).

[References]

[1] Patent: WO2004/46133, 2004, A1. Location in patent: Page 31
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