Iodopyrazine
Iodopyrazine Basic information
- Product Name:
- Iodopyrazine
- Synonyms:
-
- IODOPYRAZINE
- 2-IODOPYRAZINE 97%
- Iodopyrazine,97%
- 2-Iodo-1,4-diazine
- 2-Iodopyrazine,95%
- 2-IODOPYRAZINE
- Iodopyrazine 97%
- Iodopyrazine>
- CAS:
- 32111-21-0
- MF:
- C4H3IN2
- MW:
- 205.98
- Product Categories:
-
- alkyl Iodine
- Building Blocks
- Chemical Synthesis
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Organohalides
- Pyrazine
- PyrazinesHeterocyclic Building Blocks
- Building Blocks
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Pyrazines
- Halogenated
- Mol File:
- 32111-21-0.mol
Iodopyrazine Chemical Properties
- Melting point:
- 90 °C (decomp)
- Boiling point:
- 109-110 °C34 mm Hg(lit.)
- Density
- 2.086 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.655(lit.)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- -0.85±0.10(Predicted)
- form
- Crystalline Powder
- color
- White to pale yellow
- Sensitive
- Light Sensitive
- InChI
- InChI=1S/C4H3IN2/c5-4-3-6-1-2-7-4/h1-3H
- InChIKey
- OYWPFIUVDKHHGQ-UHFFFAOYSA-N
- SMILES
- C1(I)=NC=CN=C1
- CAS DataBase Reference
- 32111-21-0(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
Iodopyrazine Usage And Synthesis
Chemical Properties
Colorless to brown liquid
Synthesis
14508-49-7
32111-21-0
General procedure for the synthesis of 2-iodopyrazine from 2-chloropyrazine: a reaction mixture of 2-chloropyrazine (7.5 mL, 83 mmol), NaI (30.3 g, 202 mmol), HOAc (9.6 mL, 168 mmol) and H2SO4 (0.5 mL) in MeCN (105 mL) was heated and refluxed for 4.5 hours. Upon completion of the reaction, the solvent was removed under reduced pressure and water (120 mL) was added. The solution was alkalized with saturated NaHCO3 solution and extracted with dichloromethane (DCM) (2 x 125 mL). The DCM layers were combined, washed sequentially with saturated Na2S2O3 solution and brine, and dried over anhydrous Na2SO4. The solvent was removed under reduced pressure to give the crude 2-iodopyrazine as an oil (12.33 g, 20% yield, 71% purity).1H NMR analysis showed that the crude contained less than about 10 mol% of 2-chloropyrazine. Following the same procedure, another batch of 2-chloropyrazine (50 g, 437 mmol) was converted to the crude 2-iodopyrazine (~65 g). The two crude batches were combined and distilled under reduced pressure (ca. 0.75 Torr, boiling point 47 °C) to give 64 g of pure 2-iodopyrazine (60% yield).1H-NMR (CDCl3, 300 MHz) δ 8.40 (dd, J = 1.8, 2.4 Hz, 1H), 8.51 (d, J = 2.4 Hz, 1H), 8.87 (d, J = 1.5 Hz, 1H).
References
[1] Tetrahedron, 1998, vol. 54, # 33, p. 9701 - 9710
[2] Patent: WO2009/114313, 2009, A2. Location in patent: Page/Page column 15
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- Iodopyrazine