HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate → N-(3-aminobutan-2-yl)-2-hydroxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate | HCID 67174902 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-aminobutan-2-yl)-2-hydroxybenzamide | HCID 59193173 | 86% |
Reaction Steps
A mixture of benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate (3.2 g, 9.36 mmol) and 10% Pd/C (0.32 g) in MeOH (120 mL) was stirred under a H2 (1 atm) atmosphere (RT, 16 h). The mixture was filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with MeOH-DCM (0-20%) to afford N-(3-aminobutan-2-yl)-2-hydroxybenzamide (1.67 g, 86%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735378B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-0990dba4e21146c9a235f9c8a122dac4 |
| Source note | uspto-grants-2014_05 |