HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → tert-butyl N-hydroxycarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-hydroxycarbamate | HCID 97534 | — |
Reaction Steps
Boc anhydride (5.91 g, 0.026 mole) was added in one portion to a stirred solution of amino alcohol in anhydrous DCM (150 mL), and the reaction mixture stirred at ambient temperature under argon for 4.5 h. Water (200 mL) was added to the reaction mixture and the organic layer separated. The organic layer was washed with brine (100 mL), dried (Na2SO4), filtered, and concentrated to give N-boc amino alcohol as a colorless liquid that became a colorless glass upon standing. The material was used without further purification. Yield: 9.0 g (quantitative); LCMS: (+) ESI: m/z=368 [M+Na]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877798B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-d23af64ae58241b38edb8414f2c41ae4 |
| Source note | uspto-grants-2014_11 |