HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Methoxy-4-nitrobenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Methyl-2-nitroanisole | HCID 97455 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Methoxy-4-nitrobenzyl bromide | HCID 12621604 | 38.6% |
Reaction Steps
A mixture of 20 g of 3-methoxy-4-nitrotoluene, 21.6 g of N-bromosuccinimide and 0.3 g of dibenzoyl peroxide in 120 ml of CCl4 is heated at reflux for 5 hours. The solvent is evaporated off under vacuum, the residue is taken up in water, extracted with DCM, washed with water, dried over Na2SO4 and evaporated under vacuum. 11.35 g of the expected product are obtained after crystallization from EtOH, mp=98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05661169 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-bd69583dd8fd4811b629cf67e43ea5ba |
| Source note | uspto-grants-1997_08 |