HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylic Acid → Benzyl 2-(2-hydroxybenzamido)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Benzyl N-(2-aminoethyl)carbamate | HCID 2794257 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 2-(2-hydroxybenzamido)ethylcarbamate | HCID 59193325 | 68.9% |
Reaction Steps
To a mixture of benzyl 2-aminoethylcarbamate (1.65 g, 8.5 mmol), imidazole (0.58 g, 8.5 mmol), salicylic acid (1.73 g, 8.5 mmol) in ethyl acetate (30 mL) was added a solution of DCC (1.75 g, 8.5 mmol) in ethyl acetate (50 mL). The mixture was stirred (RT, 16 h) and filtered. The solution was concentrated under reduced pressure and the crude product was purified by silica gel chromatography (EtOAc-PE, 0-50%) to afford benzyl 2-(2-hydroxybenzamido)ethylcarbamate as a white solid (1.84 g, 66%). Mass calculated for C17H18N2O4=314.34; found: [M+H]+=315.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846972B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-32d11ccb495648d5a8fad9eb2b77cd53 |
| Source note | uspto-grants-2014_09 |