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CAS No. : | 139115-91-6 | MDL No. : | MFCD04038542 |
Formula : | C9H19NO4 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | KSFVNEXYCULLEJ-UHFFFAOYSA-N |
M.W : | 205.25 | Pubchem ID : | 5220470 |
Synonyms : |
|
Chemical Name : | tert-Butyl (2-(2-hydroxyethoxy)ethyl)carbamate |
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P264-P270-P280-P301+P310+P330-P302+P352-P305+P351+P338-P332+P313-P337+P313-P405-P501 | UN#: | 2810 |
Hazard Statements: | H315-H319-H301 | Packing Group: | Ⅲ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
2.5 g | With sodium hydroxide; In tetrahydrofuran; toluene; at 45 - 50℃; | To a 250mL three-necked flask were added BG05 compound 3.7g (1.0eq), toluene and THF 40ml for each, bromoacetic acid 7.6 g (3.0eq), stirred, heated to 45?50°C, then added sodium hydroxide 4.4g, and reacted overnight. After the completion of the reaction under the monitor of TLC, the reaction liquid was evaporated off, the impurities were extracted with water and ethyl acetate, and the aqueous phase was adjusted to pH=3. The aqueous phase was extracted with dichloromethane, and the dichloromethane layers were combined, dried over anhydrous sodium sulfate, and then concentrated to give 2.5g BG06 oily compound. |
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