HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxy azide → tert-butyl N-hydroxycarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxy azide | HCID 18670949 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-butyl N-hydroxycarbamate | HCID 97534 | 39.2% |
Reaction Steps
A solution of 15a (9.85 g, 69.8 mmol) and t-butyldicarbonate (18.3 g, 83.8 mmol) in 50 mL of MeOH was placed in a Parr bottle with 20% Pd(OH)2 (2.0 g) and hydrogenated under 50 psi of H2 overnight. The reaction mixture was filtered through a sintered glass funnel and concentrated on a rotary evaporator. The residue was triturated with ether and the solid was collected and dried to give 3.64 g (24% yield) of Boc-amino alcohol 15b.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890915B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-d1ffc1979063447796ecd1b9b595fed9 |
| Source note | uspto-grants-2005_05 |