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CAS No. : | 40987-24-4 | MDL No. : | MFCD02682009 |
Formula : | C12H17NO2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | WQNIKIMRIXHNFF-UHFFFAOYSA-N |
M.W : | 207.27 | Pubchem ID : | 2776358 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | |
Hazard Statements: | H317-H319 | Packing Group: | |
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 |
---|---|---|
72% | Stage #1: at 215℃; for 3 h; Inert atmosphere Stage #2: at 50℃; for 2 h; Reflux |
Step 3b: Synthesis of (4-benzylmorpholin-2-yl)methanol 20.3 g of 4-benzyl-2-chloromethylmorpholine, previously obtained, 3.5 ml of water and then 45 ml of formamide (75-12-7) are placed in a 250 ml round-bottomed flask with a condenser and a thermometer and under argon. The reaction medium is heated at 215° C. at the reflux of formamide for 3 h and then cooled to 50° C. with a bath of ice-cold water. A further 3.5 ml of water are added and the refluxing is resumed for a further 2 h. After returning to ambient temperature (20° C.), the medium is poured into ice-cold water (150 ml), the resulting mixture is basified with 10M sodium hydroxide (50 ml) at pH=12, extraction is carried out twice with toluene, and the organic phases are combined and washed with a saturated NaCl solution (50 ml), dried over magnesium sulfate and brought to dryness under a vacuum of 3 mbar for 1 h. (4-Benzylmorpholin-2-yl)methanol (13.4 g) is isolated in the form of an amber oil (yield=72percent). |
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