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 | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | — |
Reaction Steps
10 g (49 mmol) of 2-bromoethylamine hydrobromide and 15 ml of triethylamine were dissolved in dichloromethane. 7.8 ml (49 mmol) of benzyl chloroformate was added to the obtained solution under cooling with ice, and they were stirred at room temperature. The reaction mixture was treated with dichloromethane as the extractant in an ordinary manner to obtain a crude product, which 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-1e5b52f86ad04e97a3127dac4b430d26 |
| Source note | uspto-grants-2008_07 |