Identification | Back Directory | [Name]
ETHYL 5-(HYDROXYMETHYL)ISOXAZOLE-3-CARBOXYLATE | [CAS]
123770-62-7 | [Synonyms]
ETHYL 5-(HYDROXYMETHYL)ISOXAZOLE-3-CARBOXYLATE ethyl 5-(hydroxymethyl)-1,2-oxazole-3-carboxylate 5-(Hydroxymethyl)isoxazole-3-carboxylic acid ethyl ester 5-(hydroxymethyl)-3-isoxazolecarboxylic acid ethyl ester 3-Isoxazolecarboxylic acid, 5-(hydroxymethyl)-, ethyl ester | [Molecular Formula]
C7H9NO4 | [MDL Number]
MFCD08273501 | [MOL File]
123770-62-7.mol | [Molecular Weight]
171.15 |
Chemical Properties | Back Directory | [Boiling point ]
338.8±32.0 °C(Predicted) | [density ]
1.280±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [pka]
13.12±0.10(Predicted) | [Appearance]
Light yellow to yellow Liquid |
Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of ethyl 5-hydroxymethylisoxazole-3-carboxylate from ethyl nitroacetate and 2-propyn-1-ol was as follows: intermediate 4- Preparation of ethyl 5-(hydroxymethyl)isoxazole-3-carboxylate. In an Ace pressure tube, 2-propyn-1-ol (1.0 mL, 16.76 mmol) and ethyl nitroacetate (3.79 mL, 33.52 mmol) were dissolved in ethanol (23.5 mL), followed by the addition of 1,4-diazabicyclo[2.2.2]octane (DABCO, 0.194 g, 1.68 mmol). The reaction tube was sealed and the reaction was heated at 80 °C for 72 hours. After completion of the reaction, it was cooled to room temperature and the reaction mixture was concentrated to dryness under reduced pressure. The resulting residue was purified by fast column chromatography on silica gel, the eluent being a mixture of dichloromethane and methanol (methanol v/v fraction 0% to 6%), resulting in ethyl 5-(hydroxymethyl)isoxazole-3-carboxylate 2.32 g in 81% yield as an oil.ESI/APCI (+): m/z 172 ([M+H]+). | [References]
[1] European Journal of Organic Chemistry, 2007, # 26, p. 4352 - 4359 [2] Journal of the American Chemical Society, 2014, vol. 136, # 48, p. 16792 - 16799 [3] Patent: WO2010/142801, 2010, A1. Location in patent: Page/Page column 147 [4] Chemistry - A European Journal, 2012, vol. 18, # 7, p. 2081 - 2093 [5] European Journal of Organic Chemistry, 2016, vol. 2016, # 27, p. 4643 - 4655 |
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