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123320-44-5

123320-44-5 Structure

123320-44-5 Structure
IdentificationBack 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 PropertiesBack 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 InformationBack Directory
[Uses]

(3-(Benzyloxy)isoxazol-5-yl)methanol is a key precursor to tetracycline antibiotics.
[Synthesis]

3-BENZYLOXYISOXAZOLE-5-CARBOXYLIC ACID METHYL ESTER

205115-22-6

[3-(benzyloxy)-1,2-oxazol-5-yl]Methanol

123320-44-5

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
Spectrum DetailBack Directory
[Spectrum Detail]

[3-(benzyloxy)-1,2-oxazol-5-yl]Methanol(123320-44-5)1HNMR
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