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 aq. KHSO4 (50 mL) and sat. aq. NaCl (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 | US07750161B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-b3a823c92c5b47b2b219f541aec75de2 |
| Source note | uspto-grants-2010_07 |