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CAS No. : | 95656-86-3 | MDL No. : | MFCD02093569 |
Formula : | C8H17NO3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | YNJCFDAODGKHAV-UHFFFAOYSA-N |
M.W : | 175.23 | Pubchem ID : | 9920508 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | 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 |
---|---|---|
61% | With dipyridinium dichromate; In N,N-dimethyl-formamide; at 0 - 23℃; for 16h;Inert atmosphere; | To a solution of PDC (68.9 g, 183 mmol) in DMF (50 mL) was added 45 (16.0 g, 92.0 mmol) in DMF (42 mL) at 0 C. The reaction was allowedto stir for 16 h while warming to 23 C. The reaction mixture waspoured over a plug of Celite with Et2O, quenched with brine (200 mL),and diluted with Et2O (700 mL). The combined Et2O layers werewashed with aq NH4Cl (2 × 200 mL), H2O (2 × 200 mL), and brine(2 × 200 mL), dried (MgSO4), filtered, and concentrated to give Boc-aminoacetone 42 as a yellow oil; yield: 10.6 g (61.0 mmol, 61%). |
52% | With sulfur trioxide pyridine complex; triethylamine; In dichloromethane; dimethyl sulfoxide; for 6h; | 2.24 g (12.7 mmol) of (2-hydroxy-propyl)-carbamic acid t-butyl ester obtained in the above step (1) was dissolved in 30 mL of dichloromethane, and then 3.6 mL (25.7 mmol) of triethylamine was dropwise added. To the resulting solution, was added a solution of 6.05 g (19 mmol) of 50% pyridine sulfur trioxide which was dissolved in 15 mL of dimethylsulf oxide. After 6 hours, 200 mL of ethyl acetate was added thereto and the reaction solution was washed with water, then an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, then the residue was purified by column chromatography to give 1.15 g (6.64 mmol) of the title compound in a yield of 52%.[376] NMR: 1H-NMR(CDCl3) delta 5.2O(1H, brs), 4.05~4.00(2H, m), 2.17(3H, s), 1.43(9H, s)[377] Mass(EI) 174(M++.) |
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