HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylic Acid → Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Benzyl 3-aminobutan-2-ylcarbamate | HCID 59193262 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate | HCID 67174902 | 40% |
Reaction Steps
To a mixture of benzyl 3-aminobutan-2-ylcarbamate (5.3 g, 23.8 mmol), 2-hydroxybenzoic acid (3.28 g, 23.8 mmol) and imidazole (1.62 g, 23.8 mmol) in EtOAc (180 mL) at 0° C. was slowly added a solution of DCC (4.90 g, 23.8 mmol) in EtOAc (20 mL). The reaction mixture was stirred (RT, 16 h), filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with PE-EA (5:1) to afford benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate (3.2 g, 40%) as a colorless oil. Mass calculated for C19H22N2O4=342.39. found: [M+H]+=343.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735379B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-24c798c8a99f464b958626c2627a6e53 |
| Source note | uspto-grants-2014_05 |