HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Tert-butyl (5-bromo-2-methoxybenzyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Tert-butyl (2-methoxybenzyl)carbamate | HCID 22926021 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl (5-bromo-2-methoxybenzyl)carbamate | HCID 22926030 | 86.6% |
Reaction Steps
6.04 g of t-butyl N-(2-methoxybenzyl)carbamate was dissolved in 50 ml of acetonitrile, and 4.6 g of N-bromosuccinimide was added. After stirring for 3 hours at room temperature, the solvent was evaporated. The residue was dissolved in ethyl acetate, and successively washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was washed with mixture solution of methyl t-butylmethyl ether and hexane, to give 6.97 g of t-butyl N-(5-bromo-2-methoxybenzyl)carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244861B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-52512523871d4e4d8e460cff3db66c96 |
| Source note | uspto-grants-2007_07 |