ChemicalBook--->CAS DataBase List--->4774-18-9

4774-18-9

4774-18-9 Structure

4774-18-9 Structure
IdentificationBack Directory
[Name]

2-(BENZYLOXY)-6-CHLOROPYRAZINE
[CAS]

4774-18-9
[Synonyms]

2-(benzyloxy)-6-chloropyraine
2-chloro-6-(phenylmethoxy)Pyrazine
Pyrazine, 2-chloro-6-(phenylmethoxy)-
[Molecular Formula]

C11H9ClN2O
[MDL Number]

MFCD08691288
[MOL File]

4774-18-9.mol
[Molecular Weight]

220.65
Chemical PropertiesBack Directory
[Boiling point ]

321.4±37.0 °C(Predicted)
[density ]

1.278±0.06 g/cm3(Predicted)
[storage temp. ]

Storage temp. 2-8°C
[pka]

-1.78±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C11H9ClN2O/c12-10-6-13-7-11(14-10)15-8-9-4-2-1-3-5-9/h1-7H,8H2
[InChIKey]

AOYRICZDNURREY-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC(OCC2=CC=CC=C2)=CN=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-(BENZYLOXY)-6-CHLOROPYRAZINE(4774-18-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,6-Dichloropyrazine

4774-14-5

Benzyl alcohol

100-51-6

2-(BENZYLOXY)-6-CHLOROPYRAZINE

4774-18-9

Benzyl alcohol (0.75 mL, 7.24 mmol) was slowly added dropwise to a cooled suspension of sodium hydride (60%, 300 mg, 7.5 mmol) in THF (20 mL) at 0 °C. After dropwise addition, stirring was continued for 30 min. Subsequently, 2,6-dichloropyrazine (999 mg, 6.71 mmol) was added and the reaction mixture was gradually warmed to room temperature and stirred overnight. After completion of the reaction, the reaction was quenched with saturated aqueous NH4Cl solution. The reaction mixture was extracted with ethyl acetate and the organic phases were combined and washed sequentially with water and brine. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the crude product 2-benzyloxy-6-chloropyrazine (1.45 g, 5.33 mmol), which could be used in the next reaction without further purification.

[References]

[1] Synlett, 2014, vol. 25, # 13, p. 1904 - 1908
[2] Patent: US4791127, 1988, A
[3] Patent: KR2016/37198, 2016, A. Location in patent: Paragraph 2821-2823
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