Molecular Formula | C11H19NO3 |
Molar Mass | 213.27 |
Density | 1.12 |
Melting Point | 50-52℃ |
Boling Point | 297.6±33.0 °C(Predicted) |
Appearance | Shape Crystalline Powder, color White |
Color | White |
pKa | -0.82±0.20(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Use | Application 1-oxa-6-aza-spirol [2.5] oct-6-formate tert-butyl ester is an organic intermediate, which can be prepared by the reaction of N-Boc-4-piperidone and trimethylsulfoxide iodide. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S22 - Do not breathe dust. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
HS Code | 29349990 |
Hazard Class | IRRITANT |
Downstream Products | 4-Aminomethyl-4-fluoro-piperidine-1-carboxylic acid tert-butyl ester |
dissolve trimethyl iodide sulfoxide (3.094g,14.06mmol,1.4eqv) in 15mL of anhydrous DMSO, add sodium hydride (0.562g,14.06mmol,1.4eqv,60% in kerosene) in three batches under the condition of ice bath, add it, stir at 0 ℃ for 30 minutes, add N-Boc-4-piperidone (2.0g,10.04mmol,1.0eqv), after adding, continue stirring at this temperature for 4 hours; Add 40mL of water, extract ethyl acetate (3 × 90mL), wash saturated salt water, dry anhydrous sodium sulfate, filter, concentrate to obtain crude product, column chromatography (PE:EA = 10:1, then PE:EA = 5:1) Compound 1-oxa-6-aza-spiro [2.5] oct-6-formate tert-butyl ester (1.285g, white waxy solid, 60% yield) was obtained.
Application | 1-oxa-6-aza-spiro [2.5] oct-6-carboxylic acid tert-butyl ester is an organic intermediate, it can be prepared by reacting N-Boc-4-piperidone with trimethyl sulfoxide iodide. |
preparation | trimethylsulfoxide iodide (3.094g,14.06mmol,1.4eqv) was dissolved in 15ml of anhydrous DMSO, under the condition of ice bath, sodium hydride (0.562g,14.06mmol,1.4eqv,60% in kerosene) was added in three portions, and the mixture was stirred at 0 ° C. For 30 minutes, n-Boc-4-piperidone (2.0g,10.04mmol,1.0eqv) was added and stirring was continued at this temperature for 4 hours; Water (40ml) was added and the mixture was extracted with ethyl acetate (3 × 90ml), saturated brine washing, anhydrous sodium sulfate drying, filtration, concentration to obtain crude, column chromatography (PE:EA = 10:1, then PE:EA = 5:1) the compound 1-oxa-6-aza-spiro [2.5] oct-6-carboxylic acid tert-butyl ester (1.285g, white waxy solid, yield 60%) was obtained. |