Basic information Safety Supplier Related

2-Mercaptobenzooxazole-6-carboxylic acid methyl ester

Basic information Safety Supplier Related

2-Mercaptobenzooxazole-6-carboxylic acid methyl ester Basic information

Product Name:
2-Mercaptobenzooxazole-6-carboxylic acid methyl ester
Synonyms:
  • Methyl 2-sulfanyl-1,3-benzoxazole-6-carboxylate
  • methyl 2-mercapto-1,3-benzoxazole-6-carboxylate
  • 2-Mercaptobenzooxazole-6-carboxylic acid methyl ester
  • Methyl 2-mercaptobenzo[d]oxazole-6-carboxylate
  • 6-Benzoxazolecarboxylic acid, 2,3-dihydro-2-thioxo-, methyl ester
  • methyl 2-sulfanylidene-3H-1,3-benzoxazole-6-carboxylate
  • 6-bromo-5-fluoro-1,3-dihydroindol-6-one
  • 5-ETHYL-7-METHOXY-BENZENESULFONYLCHLORIDE
CAS:
72752-81-9
MF:
C9H7NO3S
MW:
209.22
EINECS:
1312995-182-4
Mol File:
72752-81-9.mol
More
Less

2-Mercaptobenzooxazole-6-carboxylic acid methyl ester Chemical Properties

Boiling point:
339.9±44.0 °C(Predicted)
Density 
1.46±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
10.45±0.20(Predicted)
Appearance
White to off-white Solid
More
Less

2-Mercaptobenzooxazole-6-carboxylic acid methyl ester Usage And Synthesis

Synthesis

140-89-6

63435-16-5

72752-81-9

The general procedure for the synthesis of methyl 2-mercaptobenzo[D]oxazole-6-carboxylate from potassium ethylxanthate and methyl 4-amino-3-hydroxybenzoate was as follows: a suspension of methyl 4-amino-3-hydroxybenzoate (393 g, 2.35 mol) and potassium ethylxanthate (393 g, 2.45 mol) in pyridine (3 L) was heated and refluxed for 12 hours. Completion of the reaction was confirmed by monitoring the progress of the reaction by thin layer chromatography (TLC, unfolding agent ratio ethyl acetate/petroleum ether = 1:2). The reaction mixture was cooled to room temperature and slowly poured into four 5L flasks containing 1600mL of concentrated hydrochloric acid and 10L of ice water, respectively. After vigorous stirring for 5 minutes, the solid product was collected by filtration. The solid was washed with 1 L of water and dried in air for 30 min. The dried solid was dissolved in 10 L of ethyl acetate and the organic phase was washed sequentially with 2 L of 1N hydrochloric acid and 1 L of saturated saline. The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the target product methyl 2-mercaptobenzo[D]oxazole-6-carboxylate (390 g, 79.3% yield) as a pink solid.

References

[1] Patent: US2010/305073, 2010, A1. Location in patent: Page/Page column 21
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 15, p. 4998 - 5002
[3] Patent: WO2018/85148, 2018, A1. Location in patent: Paragraph 0114
[4] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 7, p. 1975 - 1980

2-Mercaptobenzooxazole-6-carboxylic acid methyl esterSupplier

Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Email
sales.bj@hwrkchemical.com
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Email
sales@chemreagents.com
Shanghai Paulshine Chemical Co., Ltd.
Tel
+86-021-37788663
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
China Langchem Inc.
Tel
0086-21-58956006
More
Less