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
t-Butyl N-(2-methoxybenzyl)carbamate (6.04 g) was dissolved in 50 ml of acetonitrile, and 4.6 g of N-bromosuccinimide was added thereto. The mixture was stirred at room temperature for 3 hours, and then the solvent was evaporated. The residue was dissolved in ethyl acetate and successively washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was washed with a mixed solvent of t-butyl methyl ether and hexane, to give 6.97 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687664B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-647d908904764a3f99f61637e9cb43fb |
| Source note | uspto-grants-2010_03 |