HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl(S)-3-tert-butoxycarbonylamino-2-morpholin-4-ylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bis(2-chloroethyl) ether | HCID 8115 | — |
| Reactant | Methyl 3-((tert-butoxycarbonyl)amino)-L-alaninate | HCID 7021143 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | methyl(S)-3-tert-butoxycarbonylamino-2-morpholin-4-ylpropanoate | HCID 67056346 | 24.3% |
Reaction Conditions
| Temperature | 127 °C |
|---|
Reaction Steps
2.8 g (20 mmol) of 1-chloro-2-(2-chloroethoxy)ethane are added to a solution of 5 g (20 mmol) of commercial methyl(S)-2-amino-3-tert-butoxycarbonylaminopropanoate in 65 ml of diisopropylethylamine. The reaction mixture is stirred at 127° C. for 18 h. After the addition of water, the reaction medium is extracted with ethyl acetate. The organic phases are combined, dried over sodium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on silica gel, elution being carried out with a 70/30 heptane/ethyl acetate mixture. 1.4 g (24%) of methyl(S)-3-tert-butoxycarbonylamino-2-morpholin-4-ylpropanoate are obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772478B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-1fab35d85d4e444faac3bb95a0ba71ef |
| Source note | uspto-grants-2014_07 |