HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → tert-butyl N-hydroxy-N-(2-methylpropyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | tert-butyl N-benzyloxy-N-(2-methylpropyl)carbamate | HCID 19967428 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl N-hydroxy-N-(2-methylpropyl)carbamate | HCID 19967442 | 99.1% |
Reaction Steps
Ammonium formate (7.9 g, 125 mmol) and 10% palladium on carbon (2 g) were added to a solution of tert-butyl-N-benzyloxy-N-(2-methylpropyl)carbamate (Compound 54 Part B, 6.27 g, 22.4 mmol) in ethanol (100 mL). The reaction mixture was stirred at ambient temperature for 5 hours then concentrated under vacuum at 50° C. The residue was taken up in methylene chloride, washed with water, dried with magnesium sulfate and then concentrated to provide 4.2 g of tert-butyl N-hydroxy-N-(2-methylpropyl)carbamate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05612377 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-f0ababa71772444b91273ae6bc67f214 |
| Source note | uspto-grants-1997_03 |