HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → benzyl N-(2-bromoethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | HCID 86760711 | HCID 86760711 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | — |
Reaction Steps
10 g (49 mmol) of 2-bromoethylamine bromate and 15 ml of triethylamine were dissolved in dichloromethane. 7.8 ml (49 mmol) of benzyl chloroformate was added to the solution under cooling with ice, and they were stirred at room temperature. After the treatment with dichloromethane as the extractant in an ordinary manner, the crude product was obtained. The crude product was purified by the silica gel column chromatography to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396844B1 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-bed04e71776e4e4d93bf32ce3362d66a |
| Source note | uspto-grants-2008_07 |