ChemicalBook--->CAS DataBase List--->27383-86-4

27383-86-4

27383-86-4 Structure

27383-86-4 Structure
IdentificationBack Directory
[Name]

BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER
[CAS]

27383-86-4
[Synonyms]

Methyl 2-benzoxazolecarboxylate
Methyl 1,3-benzoxazole-2-carboxylate
Methyl benzo[d]oxazole-2-carboxylate
2-Benzoxazolecarboxylic acid, Methyl ester
BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER
[Molecular Formula]

C9H7NO3
[MDL Number]

MFCD09701312
[MOL File]

27383-86-4.mol
[Molecular Weight]

177.16
Chemical PropertiesBack Directory
[Melting point ]

99 °C
[Boiling point ]

272.3±23.0 °C(Predicted)
[density ]

1.288±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

0.14±0.10(Predicted)
[Appearance]

White to light brown Solid
[InChI]

InChI=1S/C9H7NO3/c1-12-9(11)8-10-6-4-2-3-5-7(6)13-8/h2-5H,1H3
[InChIKey]

YDKNBNOOCSNPNS-UHFFFAOYSA-N
[SMILES]

O1C2=CC=CC=C2N=C1C(OC)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

Methyl Benzo[D]oxazole-2-carboxylate is used as a reactant in the preparation of benzoxazole-based oxadiazoles as antimicrobial agents.
[Synthesis]

Benzoxazole

273-53-0

Carbon dioxide

124-38-9

Iodomethane

74-88-4

BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER

27383-86-4

Catalyst (9.9 mg, 0.025 mmol, 5 mol%), potassium tert-butoxide (0.0672 g, 0.6 mmol) and DMF (3.0 mL) were added to the reaction flask under argon protection. Benzoxazole (50.7 μL, 0.5 mmol) was then added and carbon dioxide gas was passed under atmospheric pressure. The reaction mixture was stirred at 80 °C for 18 hours. After completion of the reaction, the temperature was lowered to 65 °C, iodomethane (93 μL, 1.5 mmol) was added, and stirring was continued at 65 °C for 1 h. The reaction was carried out with the aid of deionized water. At the end of the reaction, the reaction was quenched with deionized water and the reaction product was extracted with ethyl acetate. The yield of the product, methyl benzo[d]oxazole-2-carboxylate, was measured to be 95% by gas chromatography analysis. Further purification by column chromatography using ethyl acetate/petroleum ether (1:10, v/v) as the unfolding solvent gave 90% yield of the purified product.

[References]

[1] Green Chemistry, 2018, vol. 20, # 5, p. 989 - 996
[2] Organic Letters, 2010, vol. 12, # 15, p. 3567 - 3569
[3] Journal of the American Chemical Society, 2010, vol. 132, # 26, p. 8858 - 8859
[4] Patent: CN106565623, 2017, A. Location in patent: Paragraph 0021
[5] Angewandte Chemie - International Edition, 2010, vol. 49, # 46, p. 8670 - 8673
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