ChemicalBook--->CAS DataBase List--->98019-60-4

98019-60-4

98019-60-4 Structure

98019-60-4 Structure
IdentificationBack Directory
[Name]

5-ISOXAZOLEMETHANOL
[CAS]

98019-60-4
[Synonyms]

AKOS PAO-1429
5-ISOXAZOLEMETHANOL
Isoxazole-5-methanol
ISOXAZOL-5-YL-METHANOL
1,2-Oxazol-5-ylmethanol
5-(Hydroxymethyl)isoxazole
[Molecular Formula]

C4H5NO2
[MDL Number]

MFCD06738883
[MOL File]

98019-60-4.mol
[Molecular Weight]

99.09
Chemical PropertiesBack Directory
[Boiling point ]

115-125 °C(Press: 16 Torr)
[density ]

1.250
[storage temp. ]

2-8°C
[pka]

13.41±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315-H302
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
Spectrum DetailBack Directory
[Spectrum Detail]

5-ISOXAZOLEMETHANOL(98019-60-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

ISOXAZOLE-5-CARBOXYLIC ACID

21169-71-1

5-ISOXAZOLEMETHANOL

98019-60-4

To a solution of isoxazole-5-carboxylic acid (1.0 g, 8.8 mmol) in tetrahydrofuran (THF, 10 mL) was slowly added borane-THF complex (26.4 mL, 1 M in THF, 26.4 mmol) at 0 °C. The reaction mixture was stirred at room temperature and the progress of the reaction was monitored by thin layer chromatography (TLC) until isoxazole-5-carboxylic acid was completely consumed. Upon completion of the reaction, ethanol (5 mL) was added slowly at 0 °C to quench the reaction. The reaction mixture was transferred to a dispensing funnel and partitioned with ethyl acetate and water. The organic phase was separated and the aqueous phase was back-extracted with ethyl acetate. All organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product isoxazol-5-ylmethanol. The crude product was purified by silica gel column chromatography with the eluent of petroleum ether/ethyl acetate (2:1, v/v) to give the pure isoxazol-5-ylmethanol (670 mg, 77.0% yield) as a light yellow oil. The product was analyzed by liquid chromatography-mass spectrometry (LC-MS) with a retention time of 0.329 min and a molecular ion peak (MH+) of 100.

[References]

[1] Patent: WO2014/143799, 2014, A2. Location in patent: Page/Page column 400; 401
[2] Patent: WO2013/30138, 2013, A1. Location in patent: Page/Page column 153; 15415
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