5-broMo-6-(trifluoroMethyl)pyriMidin-4-ol

5-broMo-6-(trifluoroMethyl)pyriMidin-4-ol Property

storage temp. 

2-8°C

Appearance

white solid

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H312Harmful in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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

P312Call a POISON CENTER or doctor/physician if you feel unwell.

P321Specific treatment (see … on this label).

P322Specific measures (see …on this label).

P330Rinse mouth.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

P363Wash contaminated clothing before reuse.

P501Dispose of contents/container to..…

5-broMo-6-(trifluoroMethyl)pyriMidin-4-ol Chemical Properties,Usage,Production

Synthesis

General procedure for the synthesis of 5-bromo-6-trifluoromethylpyrimidin-4-one from 6-trifluoromethyl-4-hydroxypyrimidine: To a solution of acetic acid (2 mL) containing 8-(bromomethyl)pyrido[2,3-d]pyridazin-5(6H)-one (0.3 g, 1.8 mmol) was added CH3COOK (0.54 g, 5.5 mmol). Subsequently, a solution of bromine (Br2) in acetic acid (1 mL) was added dropwise to the reaction mixture. The reaction mixture was heated to 80 °C and stirred overnight. Upon completion of the reaction, the mixture was cooled to room temperature, diluted with ethyl acetate (EtOAc), washed sequentially with water and brine, dried over anhydrous sodium sulfate (Na2SO4), and finally the target product, 5-bromo-6-(trifluoromethyl)-4(3H)-pyrimidinedione (0.3 g), was obtained by evaporation of the solvent.

References

[1] European Journal of Organic Chemistry, 2004, # 17, p. 3714 - 3718
[2] Patent: WO2014/58747, 2014, A1. Location in patent: Page/Page column 61
[3] Patent: WO2015/153304, 2015, A1. Location in patent: Page/Page column 25