4-Bromo-3,5-dimethylisoxazole CAS 10558-25-5

Introduction:Basic information about 4-Bromo-3,5-dimethylisoxazole CAS 10558-25-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

4-Bromo-3,5-dimethylisoxazole Basic information

Product Name:4-Bromo-3,5-dimethylisoxazole
Synonyms:BUTTPARK 33\06-98;4-BROMO-3,5-DIMETHYLISOXAZOLE;4-BROMO-3,5-DIMETHYLISOXAZOLE 97%;Isoxazole, 4-broMo-3,5-diMethyl-;4-Bromo-3,5-dimethylisoxazole, tech.;4-Bromo-3,5-dimethylisoxazole,97%;4-Bromo-3,5-dimethylisoxa...;TIMTEC-BB SBB003784
CAS:10558-25-5
MF:C5H6BrNO
MW:176.01
EINECS:000-000-0
Product Categories:Halogenated Heterocycles;Heterocyclic Building Blocks;Isoxazoles;IsoxazolesBuilding Blocks;Oxazole&Isoxazole;blocks;Bromides;Oxazoles
Mol File:10558-25-5.mol

4-Bromo-3,5-dimethylisoxazole Chemical Properties

Boiling point 176 °C(lit.)
density 1.478 g/mL at 25 °C(lit.)
refractive index n20/D 1.486(lit.)
Fp >230 °F
storage temp. 2-8°C
pka-2.35±0.28(Predicted)
form clear liquid
color Colorless to Light orange to Yellow
Sensitive Light Sensitive
BRN 108522
InChIInChI=1S/C5H6BrNO/c1-3-5(6)4(2)8-7-3/h1-2H3
InChIKeyGYHZPSUAMYIFQD-UHFFFAOYSA-N
SMILESO1C(C)=C(Br)C(C)=N1
CAS DataBase Reference10558-25-5(CAS DataBase Reference)

Safety Information

Safety Statements 24/25
WGK Germany 3
Hazard Note Keep Cold/Light Sensitive
HS Code 29349990
Storage Class10 - Combustible liquids

4-Bromo-3,5-dimethylisoxazole Usage And Synthesis

Chemical Propertiesclear colorless to light yellow liquid
Uses4-Bromo-3,5-dimethylisoxazole may be used in the preparation of (tert-butyldimethylsilyl)-(3,5-dimethylisoxazol-4-yl)phenylamine and 3,3′,5,5′-tetramethyl-4,4′-diisoxazole.[21}
General Description4-Bromo-3,5-dimethylisoxazole is also known as 3,5-dimethyl-4-bromoisoxazole.
Synthesis

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10558-25-5

The general procedure for the synthesis of 4-bromo-3,5-dimethylisoxazole from 3,5-dimethylisoxazole is as follows:1. Preparation of intermediate 105 (4-bromo-3,5-dimethyl-1,2-oxazole): DMF (53 mL) was added to a 250 mL round-bottomed flask fitted with a magnetic stirrer.2. 3,5-dimethyl-1,2-oxazole (5.3 g, 54.57 mmol) and N-iodosuccinimide (11.659 g, 65.49 mmol) were sequentially added to the stirred DMF.3. After completion of the addition, the reaction mixture was heated to 75°C and maintained for 3 hours.4. Upon completion of the reaction, the mixture was diluted with ethyl acetate (100 mL).5. The organic layer was washed sequentially with saturated NaHCO3 solution (100 mL), sodium thiosulfate solution (100 mL), water (200 mL) and brine (100 mL).6. The organic layer was dried over anhydrous Na2SO4 and then concentrated under reduced pressure to remove the solvent to afford the target product 4-bromo-3,5-dimethyl-1,2-oxazole (6.1 g, 63.4% yield).

References[1] Patent: WO2012/11125, 2012, A1. Location in patent: Page/Page column 148; 149
[2] Rend. Ist. lomb., 1936, vol. 69, p. 587,600

4-Bromo-3,5-dimethylisoxazole Preparation Products And Raw materials

Raw materials3,5-Dimethylisoxazole-->Ethyl acetate-->Sodium bicarbonate-->N,N-Dimethylformamide-->N-Bromosuccinimide
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