2-BROMO-5-METHOXYANILINE
2-BROMO-5-METHOXYANILINE Basic information
- Product Name:
- 2-BROMO-5-METHOXYANILINE
- Synonyms:
-
- 2-BROMO-5-METHOXYANILINE
- 4-Bromo-3-amino anisole
- 2-bromo-5-methoxybenzenamine
- 2-Bromo-5-Methoxyaniline (In HCl salt form)
- 2-BROMO-5-METHOXYANI
- 2-BroMo-5-Methoxy-phenylaMine
- 2-Bromo-5-methoxyaniline 97%
- 3-Amino-4-bromoanisole, 6-Bromo-m-anisidine
- CAS:
- 59557-92-5
- MF:
- C7H8BrNO
- MW:
- 202.05
- EINECS:
- 611-853-9
- Product Categories:
-
- Phenyls & Phenyl-Het
- Amines
- Phenyls & Phenyl-Het
- Anilines, Amides & Amines
- Anisoles, Alkyloxy Compounds & Phenylacetates
- Bromine Compounds
- Mol File:
- 59557-92-5.mol
2-BROMO-5-METHOXYANILINE Chemical Properties
- Melting point:
- 189-190°C
- Boiling point:
- 280.1±20.0 °C(Predicted)
- Density
- 1.531±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 2.11±0.10(Predicted)
- form
- solid
- Appearance
- Brown to black Solid-liquid mixture
- CAS DataBase Reference
- 59557-92-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- HS Code
- 29222990
2-BROMO-5-METHOXYANILINE Usage And Synthesis
Uses
2-Bromo-5-methoxyaniline is used as a synthetic material intermediate for the preparation of epidermal growth factor receptor inhibitors, urolithin derivatives and melatonergic ligands. It is also an OLED intermediate for organic electroluminescent devices.
Synthesis
5344-78-5
59557-92-5
1. 4-Bromo-3-nitroanisole (1.71 g, 7.2 mmol, 1 eq.) was dissolved in a solvent mixture of ethanol (7 mL) and water (5 mL). 2. To the above solution was added iron powder (2.00 g, 35.7 mmol, 5 eq.) and ammonium chloride (1.53 g, 28.6 mmol, 4 eq.). 3. The reaction mixture was heated to reflux for 2 hours. 4. Upon completion of the reaction, the black organic phase was extracted with ether (4 x 100 mL). 5. The organic phase was separated to give 2-bromo-5-methoxyaniline in 95% yield as a green solid. 6. 2-Bromo-5-methoxyaniline (1.50 g, 7.4 mmol, 1 eq.), the crude product, was dissolved in concentrated hydrochloric acid (7 mL) at 0 °C. 7. To the above solution was added dropwise an aqueous solution of sodium nitrite (0.5 g, 7.2 mmol, 1 eq.) (5 mL) at 0 °C. 8. Continue stirring for 5 hours at 0 °C to form the diazonium salt. 9. In another flask, treat water (8 mL) with thionyl chloride (2.2 mL, 30.3 mmol, 4 eq.) at 0 °C. 10. Stirring was continued for 1 hour at 0 °C. 11. Wash the aqueous phase with ethyl acetate (6 x 50 mL). 12. Combine the organic phases and dry with magnesium sulfate. 13. The solvent was removed under pressure and the product was purified by column chromatography (n-hexane-ethyl acetate, 5:1) to afford the target product S5 (1.50 g, 46%) as a yellow oil. 14. The Rf value of the product was 0.3 (n-hexane-ethyl acetate, 5:1), which was in agreement with the data reported in the literature.
References
[1] Chemistry - A European Journal, 2017, vol. 23, # 42, p. 9996 - 10000
[2] Journal of Medicinal Chemistry, 1995, vol. 38, # 6, p. 950 - 957
[3] Organic Letters, 2015, vol. 17, # 4, p. 802 - 805
[4] Tetrahedron Letters, 2017, vol. 58, # 48, p. 4559 - 4562
[5] Journal of the American Chemical Society, 1994, vol. 116, # 26, p. 11797 - 11810
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2-BROMO-5-METHOXYANILINE(59557-92-5)Related Product Information
- 2-Bromo-5-methylpyridine
- 2-BROMO-5-METHOXYPYRIDINE
- 2-Bromo-6-(trifluoromethyl)pyridine
- 2-Bromo-6-methylpyridine
- 2-BROMO-5-IODOBENZYL ALCOHOL
- 2-Bromo-5-nitropyridine
- 2-Bromo-5-(trifluoromethyl)pyridine
- 5-Amino-2-bromopyridine
- 6-Bromonicotinic acid
- 2-Bromo-5-chloropyridine
- 2-Bromo-5-fluoropyridine
- 5-Bromo-2-methoxyaniline, HCl
- 5-BROMO-2-METHOXYANILINE
- 2-BROMO-4-METHOXYANILINE
- 2-Bromo-5-methoxyaniline, HCl
- 2-bromo-5-aminoanisole(4-bromo-3-methoxyaniline),4-BROMO-3-METHOXYANILINE, 98+%,4-BROMO-3-METHOXYANILINE,4-Bromo-3-methoxyaniline, 97+%
- 4-BROMO-2-METHOXYANILINE[2-AMINO-5-BROMOANISOLE] ,4-BROMO-2-METHOXYANILINE
- 2-BROMO-5-METHOXYANILINE SULPHATE