HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 5-(Boc-amino)-2-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl (4-methyl-3-nitrophenyl)carbamate | HCID 18954623 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(Boc-amino)-2-methylaniline | HCID 24699786 | 99.7% |
Reaction Steps
To a solution of tert-butyl(4-methyl-3-nitrophenyl)carbamate (10.1 g, 39.8 mmol) in ethanol (60 mL)/tetrahydrofuran (20 mL) was added 10% palladium-carbon (2.12 g), and the mixture was stirred at room temperature under a hydrogen atmosphere (3 atm) for 22 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (8.82 g, 99%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344135B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-2fdbb0f5f4ce4f92b9af48c8ab3c7227 |
| Source note | uspto-grants-2013_01 |