HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-(Bromomethyl)-4-chloro-2-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-CHLORO-2-METHYLANISOLE | HCID 292858 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(Bromomethyl)-4-chloro-2-methoxybenzene | HCID 22327474 | 67.4% |
Reaction Steps
303 g of 4-chloro-2-methoxytoluene are dissolved in 1665 ml of carbon tetrachloride and, together with 355 g of N-bromosuccinimide, heated at reflux for 2 h while 4.0 g of AIBN are added. The solid is filtered off and washed with a small amount of carbon tetrachloride, the filtrate is concentrated, and the residue which remains is fractionated. 307 g of colorless oil are obtained (b.p. 103° C./1.5 mbar, m.p. 42-45° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06939888B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-6e685fd7aaf147d3823ae9474d0ce132 |
| Source note | uspto-grants-2005_09 |