4-Amino-3,5-dibromobenzonitrile

4-Amino-3,5-dibromobenzonitrile Property

Melting point:

124-126℃

Boiling point:

312℃

Density 

2.12

Flash point:

113℃

storage temp. 

2-8°C(protect from light)

pka

-2.40±0.10(Predicted)

Appearance

Off-white to light yellow Powder

Safety

HS Code 

2926907090

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

4-Amino-3,5-dibromobenzonitrile Chemical Properties,Usage,Production

Synthesis

Preparation of Example 25 4-amino-3,5-dibromobenzonitrile (STR37): To a stirred solution of 100 mg (0.847 mmol) of p-aminobenzonitrile dissolved in 3.6 mL of dioxane was sequentially added 356 μL (1.78 mmol) of 5N sodium hydroxide solution and an appropriate amount (1.78 mmol) of bromine under ice-bath cooling conditions. After removing the ice water bath, the reaction mixture was continued to stir for 1.5 hours. Subsequently, 21.8 μL (0.423 mmol) of bromine was added to ensure that the reaction was complete and stirring was continued for 10 minutes. The reaction mixture was partitioned with ethyl acetate and ice water to separate the organic phase. The organic phase was sequentially washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by silica gel plate chromatography using hexane-ethyl acetate (7:3, v/v) as eluent gave 175 mg (74%) of the target product 4-amino-3,5-dibromobenzonitrile. The product was characterized by NMR (CDCl3): δ 5.1 (broad peak, 2H), 7.66 (single peak, 2H).

References

[1] RSC Advances, 2016, vol. 6, # 93, p. 90184 - 90187
[2] Journal fuer Praktische Chemie (Leipzig), 1986, vol. 328, # 4, p. 497 - 514
[3] Journal of Organic Chemistry, 1998, vol. 63, # 5, p. 1555 - 1565
[4] Journal of the American Chemical Society, 1960, vol. 82, p. 3454 - 3456
[5] Synthesis (Germany), 2013, vol. 45, # 11, p. 1497 - 1504