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METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE

Basic information Safety Supplier Related

METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE Basic information

Product Name:
METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE
Synonyms:
  • METHYL 2-(CHLOROMETHYL)-1,3-OXAZOLE-4-CARBOXYLATE
  • METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE
  • METHYL 2-CHLOROMETHYL-4-OXAZOLECARBOXYLATE
  • 2-CHLOROMETHYL-OXAZOLE-4-CARBOXYLIC ACID METHYL ESTER
  • 4-Oxazolecarboxylic acid, 2-(chloroMethyl)-, Methyl ester
  • 2-(Chloromethyl)-4-(methoxycarbonyl)-1,3-oxazole
  • Methyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate 97%
  • Methyl2-(chloromethyl)-1,3-oxazole-4-carboxylate97%
CAS:
208465-72-9
MF:
C6H6ClNO3
MW:
175.57
Product Categories:
  • pharmacetical
  • Building Blocks
  • Oxazole
Mol File:
208465-72-9.mol
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METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE Chemical Properties

Melting point:
74 °C
Boiling point:
230℃
Density 
1.339
Flash point:
93℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-2.41±0.10(Predicted)
color 
Off-white
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
22-26-36/37/39-45
Hazard Note 
Corrosive
HS Code 
2934999090
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METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE Usage And Synthesis

Synthesis

3018-12-0

5680-80-8

208465-72-9

GENERAL STEPS: Sodium methanolate (25.00 mg, 0.46 mmol) was dissolved in anhydrous methanol (4.50 mL) and dry dichloromethane (30.00 mL) under nitrogen protection and cooled to 0 °C. Dichloroacetonitrile (5.00 g, 45.50 mmol) was slowly added to this stirred solution and stirring was continued for 1 hour at 0°C. Subsequently, L-serine methyl ester hydrochloride (7.00 g, 45.50 mmol) was added and the reaction mixture was warmed to 25 °C and stirred for 12 hours. Upon completion of the reaction, water was added and the aqueous phase was extracted with dichloromethane (3 x 25.00 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was dissolved in dichloromethane (50.00 mL) and N,N-diisopropylethylamine (11.90 mL, 68.30 mmol) was added. The reaction mixture was stirred at 50 °C for 5 hours, followed by continued stirring at 25 °C for 12 hours. At the end of the reaction, water was added and the aqueous phase was extracted with dichloromethane (3 x 25.00 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The product did not require further purification (quantitative yield).ESI-MS m/z: 176 [M + H]+, 198 [M + Na]+; 1H NMR (300 MHz, CDCl3) δ 3.92 (s, 3H), 4.63 (s, 2H), 8.25 (s, 1H).

References

[1] Tetrahedron Letters, 2016, vol. 57, # 8, p. 920 - 923

METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATESupplier

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METHYL (2-CHLOROMETHYL)OXAZOLE-4-CARBOXYLATE(208465-72-9)Related Product Information