| Identification | Back Directory | [Name]
[3-(benzyloxy)-1,2-oxazol-5-yl]Methanol | [CAS]
123320-44-5 | [Synonyms]
EOS-61969 (3-(Benzyloxy)isoxazol-5-yl)Methanol [3-(benzyloxy)-1,2-oxazol-5-yl]Methano [3-(benzyloxy)-1,2-oxazol-5-yl]Methanol 5-Isoxazolemethanol, 3-(phenylmethoxy)- (3-phenylmethoxy-1,2-oxazol-5-yl)methanol | [Molecular Formula]
C11H11NO3 | [MDL Number]
MFCD23135734 | [MOL File]
123320-44-5.mol | [Molecular Weight]
205.21 |
| Chemical Properties | Back Directory | [Boiling point ]
396.6±32.0 °C(Predicted) | [density ]
1.251±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
13.12±0.10(Predicted) | [Appearance]
White to off-white Solid |
| Hazard Information | Back Directory | [Uses]
(3-(Benzyloxy)isoxazol-5-yl)methanol is a key precursor to tetracycline antibiotics. | [Synthesis]
General procedure for the synthesis of (3-(benzyloxy)isoxazol-5-yl)methanol from methyl 3-(benzyloxy)isoxazole-5-carboxylate: to a solution of methyl 3-(benzyloxy)isoxazole-5-carboxylate (2.33 g, 9.99 mmol, 1.00 eq.) in methanol (50 mL) was added sodium borohydride (756 mg, 19.98 mmol, 2.00 equivalent). The reaction mixture was stirred at 15 °C for 3 hours. The progress of the reaction was monitored by thin layer chromatography (TLC, unfolding agent ratio of petroleum ether:ethyl acetate = 5:1) to confirm the completion of the reaction. The reaction mixture was slowly poured into 0.2 M hydrochloric acid solution (200 mL) and extracted with ethyl acetate (150 mL x 2). The organic phases were combined, washed with saturated saline (200 mL × 2), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give (3-(benzyloxy)isoxazol-5-yl)methanol (1.85 g, 9.02 mmol, 90% yield) as a colorless oil.LC-MS (ESI) m/z: 206.1 [M+H]+. | [References]
[1] Patent: WO2018/140809, 2018, A1. Location in patent: Paragraph 00443; 00551; 00554; 00555 [2] European Journal of Organic Chemistry, 1998, # 3, p. 473 - 479 [3] Patent: WO2012/87833, 2012, A1. Location in patent: Page/Page column 133 [4] Journal of Medicinal Chemistry, 2015, vol. 58, # 23, p. 9133 - 9153 [5] Patent: WO2008/127361, 2008, A2. Location in patent: Page/Page column 89 |
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