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METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE

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METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE Basic information

Product Name:
METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE
Synonyms:
  • METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE
  • 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
  • 4-Bromo-3-hydroxy-2-(methoxycarbonyl)thiophene
  • methyl 3-hydroxy-4-bromo-2-thiophenecarboxylate
  • (4-bromo-3-oxo-2-thiophenylidene)-methoxymethanolate
  • 2-Thiophenecarboxylic acid, 4-bromo-3-hydroxy-, methyl ester
  • METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE ISO 9001:2015 REACH
  • methyl-3-hydroxy-4-bromo thiophen-2-carboxylate
CAS:
95201-93-7
MF:
C6H5BrO3S
MW:
237.07
Product Categories:
  • Esters
  • Thiophenes & Benzothiophenes
  • Thiophenes & Benzothiophenes
Mol File:
95201-93-7.mol
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METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE Chemical Properties

Melting point:
79-80°C
Boiling point:
247.9±35.0℃ (760 Torr)
Density 
1.803±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
103.7±25.9℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
7.93±0.15(Predicted)
Appearance
White to off-white Solid
Water Solubility 
Sparingly Soluble in water 0.95 g/L @ 25°C.
InChI
InChI=1S/C6H5BrO3S/c1-10-6(9)5-4(8)3(7)2-11-5/h2,8H,1H3
InChIKey
UFTXASQYKJFRKI-UHFFFAOYSA-N
SMILES
C1(C(OC)=O)SC=C(Br)C=1O
CAS DataBase Reference
95201-93-7
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-37/39
HS Code 
2934999090

MSDS

  • Language:English Provider:ALFA
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METHYL 4-BROMO-3-HYDROXYTHIOPHENE-2-CARBOXYLATE Usage And Synthesis

Uses

The synthesis of the thienopyranone scaffold began with the alkylation of methyl 4-bromo-3-hydroxythiophene-2-carboxylate with N-acetylmorpholine.

Synthesis

5118-06-9

95201-93-7

General procedure for the synthesis of methyl 4-bromo-3-hydroxythiophene-2-carboxylate from methyl 3-hydroxy-2-thiophenecarboxylate: 3.24 mL (63.2 mmol) of bromine was slowly added to a solution of 10 g (63.2 mmol) of methyl 3-hydroxy-2-thiophenecarboxylate in 22 mL of acetic acid and the reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the reaction solution was poured into 50 mL of water and extracted with 50 mL of dichloromethane. The organic phases were combined, washed twice with 50 mL of water and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure to give the crude product. The crude product was purified by rapid chromatography on silica gel (eluent: dichloromethane/petroleum ether, 1:2) to give 11.3 g methyl 4-bromo-3-hydroxythiophene-2-carboxylate in 76% yield. The melting point of the product was 86 °C. 1H NMR (CDCl3): δ 3.92 (s, 3H), 7.38 (s, 1H), 9.74 (s, 1H). 13C NMR (CDCl3): δ 52.2, 102.6, 103.8, 128.1, 160.4, 165.8. MS (EI): m/z = 236 (M+.). .

References

[1] Tetrahedron Letters, 2009, vol. 50, # 35, p. 5005 - 5008
[2] Tetrahedron Letters, 2011, vol. 52, # 12, p. 1288 - 1291
[3] Synthesis, 1984, vol. NO. 10, p. 847 - 850
[4] Tetrahedron Letters, 2017, vol. 58, # 26, p. 2537 - 2541
[5] Patent: US4748183, 1988, A

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