HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl succinimido carbonate → benzyl N-(2-bromoethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-(2-bromoethyl)carbamate | HCID 278694 | — |
Reaction Steps
2-Bromoethylamine hydrobromide (15 g, 73 mmol) and N-(benzyloxycarbonyloxy)succinimide (15.5 g, 62 mmol) are suspended in CH2Cl2 (150 mL) at 0° C. TEA (9 mL, 65 mmol) is added slowly keeping the temperature at 0° C. After 1 h the mixture is washed with 0.5M aqueous KHSO4 (50 mL) and brine (50 mL), the organic phase is dried (Na2SO4), filtered and evaporated to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375227B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-631fc1964fdf4380b5d012b9551c5490 |
| Source note | uspto-grants-2008_05 |