ChemicalBook--->CAS DataBase List--->1380089-33-7

1380089-33-7

1380089-33-7 Structure

1380089-33-7 Structure
IdentificationBack Directory
[Name]

(4-BROMO-3-METHYLISOXAZOL-5-YL)METHYL ACETATE
[CAS]

1380089-33-7
[Synonyms]

(4-BROMO-3-METHYLISOXAZOL-5-YL)METHYL ACETATE
5-Isoxazolemethanol, 4-bromo-3-methyl-, 5-acetate
[Molecular Formula]

C7H8BrNO3
[MDL Number]

MFCD24387374
[MOL File]

1380089-33-7.mol
[Molecular Weight]

234.05
Chemical PropertiesBack Directory
[Boiling point ]

289.6±35.0 °C(Predicted)
[density ]

1.552±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-2.86±0.38(Predicted)
[InChI]

InChI=1S/C7H8BrNO3/c1-4-7(8)6(12-9-4)3-11-5(2)10/h3H2,1-2H3
[InChIKey]

USGKSLUGKUUZSM-UHFFFAOYSA-N
[SMILES]

C(OCC1ON=C(C)C=1Br)(=O)C
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

(4-BROMO-3-METHYLISOXAZOL-5-YL)METHYL ACETATE(1380089-33-7)FT-IR
Hazard InformationBack Directory
[Synthesis]

5-Isoxazolemethanol,3-methyl-,acetate(ester)(9CI)

43214-88-6

(4-BROMO-3-METHYLISOXAZOL-5-YL)METHYL ACETATE

1380089-33-7

General procedure for the synthesis of (4-bromo-3-methylisoxazol-5-yl)methyl acetate from 3-methyl-5-isoxazolemethanol acetate: To a solution of (3-methylisoxazol-5-yl)methyl acetate (0.979 g, 6.31 mmol) in acetic acid (10 mL, 175 mmol) was added sequentially N-bromosuccinimide (1.30 g, 7.30 mmol) and sulfuric acid (0.65 mL, 12.19 mmol). The reaction mixture was heated to 110 °C and maintained for 1 hour. Upon completion of the reaction, the mixture was cooled to room temperature and slowly poured into a beaker containing ice and saturated sodium bicarbonate solution. The two-phase mixture was vigorously stirred and the basic aqueous phase (pH 8-9) was subsequently extracted with ethyl acetate (2 x 15 mL). The organic phase was washed sequentially with 2% sodium thiosulfate solution and brine (20 mL), dried over anhydrous sodium sulfate and concentrated to give a light yellow oil. The crude product was purified by a Biotage purification system (isocratic elution, 10% ethyl acetate: 90% hexane) to afford the title compound (4-bromo-3-methylisoxazol-5-yl)methyl acetate (1.30 g, 5.55 mmol, 88% yield) as a colorless to light yellow oil. lc/ms m/z 234 [M + H]+.

[References]

[1] Patent: WO2012/75383, 2012, A2. Location in patent: Page/Page column 82
[2] ACS Medicinal Chemistry Letters, 2013, vol. 4, # 9, p. 835 - 840
[3] Patent: WO2013/184878, 2013, A1. Location in patent: Paragraph 00241; 00242
[4] Patent: WO2013/184876, 2013, A1. Location in patent: Paragraph 00144; 00147; 00148
[5] Patent: WO2016/97870, 2016, A1. Location in patent: Paragraph 0168
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