Identification | Back 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 Properties | Back 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 |
Hazard Information | Back Directory | [Synthesis]
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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