HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl succinimido carbonate → N-benzyloxycarbonyl-N-diethoxyethyl-6-(phenylbutoxy)hexylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | N-diethoxyethyl-6-(4-phenylbutoxy)hexylamine | HCID 69996075 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-benzyloxycarbonyl-N-diethoxyethyl-6-(phenylbutoxy)hexylamine | HCID 69994289 | 100.2% |
Reaction Steps
To a solution of 2,39 g (6,55 mmol) N-diethoxyethyl-6-(4-phenylbutoxy)hexylamine in 25 ml acetone is added 1.59 g (7.07 mmol) N-(benzyloxycarbonyloxy)succinimide. After allowing the mixture to stir for 2 hr at room temperature, acetone is removed by evaporation and 30 ml AcOEt are added thereto. The resulting mixture is washed three times with 30 ml H2O. Once separated, the AcoEt phase is dried on anhydrous Na2SO4 and evaporated to dryness, thereby yielding 3.28 g (99%) N-benzyloxycarbonyl-N-diethoxyethyl-6-(phenylbutoxy)hexylamine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06388134B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-1bafafeb775d410ea20369b1fbfaba38 |
| Source note | uspto-grants-2002_05 |