Basic information Safety Supplier Related

METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATE

Basic information Safety Supplier Related

METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATE Basic information

Product Name:
METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATE
Synonyms:
  • METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATE
  • methyl 5-bromo-6-oxopyran-3-carboxylate
  • 2H-Pyran-5-carboxylic acid, 3-bromo-2-oxo-, methyl ester
CAS:
42933-07-3
MF:
C7H5BrO4
MW:
233.02
Product Categories:
  • Esters
  • Ring Systems
Mol File:
42933-07-3.mol
More
Less

METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATE Chemical Properties

Boiling point:
285.4±40.0 °C(Predicted)
Density 
1.812±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to light yellow Solid
More
Less

Safety Information

HS Code 
2932209090
More
Less

METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATE Usage And Synthesis

Synthesis

6018-41-3

42933-07-3

General procedure for the synthesis of methyl 3-bromo-2-oxo-2H-pyran-5-carboxylate from methyl coumalate: Pyridine tribromide (8.09 g, 25.3 mmol, 1.3 eq.) and a stirrer were added to a 50 mL round-bottomed flask equipped with a charging funnel. Methyl coumalate (3.0 g, 19.5 mmol, 1 eq.) was placed in the addition funnel. The system was evacuated three times and backfilled with argon. Seventeen mL of acetic acid was added to the flask and 10 mL of acetic acid was added to the addition funnel. The reaction flask was heated to reflux. A solution of methyl coumalate in acetic acid was added slowly and dropwise. After 4 hours of reaction, cool to room temperature and dilute the reaction mixture with deionized water. The organic and aqueous layers were separated by solvent extraction with a 1:1 ethyl acetate/hexane mixture. The organic layer was washed sequentially with deionized water (twice) and saturated saline (once) and then dried over anhydrous sodium sulfate. The desiccant was removed by filtration and the organic solvent was removed by rotary evaporation. The resulting crude product was carefully diluted with saturated aqueous sodium bicarbonate. The precipitated solid was collected by vacuum filtration. The filter cake was ground with additional sodium bicarbonate and water and dried to give 3.76 g (16.1 mmol, 83% yield) of the target product, methyl 3-bromo-2-oxo-2H-pyran-5-carboxylate, as a light yellow solid. Mass spectrometry (ESI+) analysis showed m/z = 233/235 [M+H]+.

References

[1] Patent: US2016/168140, 2016, A1. Location in patent: Paragraph 1172
[2] Patent: WO2004/792, 2003, A1. Location in patent: Page 16
[3] Organic Process Research and Development, 2003, vol. 7, # 1, p. 74 - 81
[4] Chemische Berichte, 1901, vol. 34, p. 1994
[5] Tetrahedron Letters, 1997, vol. 38, # 30, p. 5375 - 5378

METHYL 3-BROMO-2-OXO-2H-PYRAN-5-CARBOXYLATESupplier

Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Email
product02@bidepharm.com
Nanjing Chalf-Pharm Technology Co., Ltd.
Tel
025-57018978 18251899859
Email
sales@chalf-pharm.com
Jiaxing Rich Biological Technology Co., Ltd.
Tel
0573-11111111-1111 18969316891
Email
richmol@163.com