HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-tert-Butyl (oxiran-2-ylmethyl)carbamate → (3-Amino-2-hydroxy-propyl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-tert-Butyl (oxiran-2-ylmethyl)carbamate | HCID 10464779 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3-Amino-2-hydroxy-propyl)-carbamic acid tert-butyl ester | HCID 86639750 | — |
Reaction Steps
(R)-1-Oxiranylmethylcarbamic acid tert-butyl ester (2.26 g, 13.05 mmol) obtained in Step 2 above was dissolved in ethanol (15 ml), and then 28% ammonia water (6 ml) was added thereto at room temperature. After the solution was stirred at room temperature for 1.5 hour, the solvent was distilled off under reduced pressure. After the resulting residue was dissolved in methanol, the solvent was distilled off under reduced pressure to give a crude product of ((S)-3-amino-2-hydroxypropyl)carbamic acid tert-butyl ester (2.38 g) as a yellow oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362236B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-57297dafbb8d47b2b63ad80ded3b37ee |
| Source note | uspto-grants-2013_01 |