HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 2,6-Dichloro-3-nitrobenzyl Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,6-Dichloro-3-nitrotoluene | HCID 97155 | — |
| Reactant | Dibromohydantoin | HCID 54068228 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2,6-Dichloro-3-nitrobenzyl Bromide | HCID 11011535 | — |
Reaction Steps
A mixture of dibromohydantoin (70 g, 0.24 mol) and AIBN (5 g) was added in portions, at 150° C., to 2,6-dichloro-3-nitrotoluene (100 g, 0.48 mol) in chlorobenzene (400 ml). A mixture of dibromohydantoin (35 g, 0.12 mol) and AIBN (2.5 g) was added once again after 1 h. After a further 1.5 h, the mixture was allowed to cool down and ethyl acetate (500 ml) was added. This mixture was washed once, in each case, with saturated Na2SO3, Na2CO3 and NaCl solution, dried (MgSO4) and concentrated, when the title compound resulted as an amorphous powder. ##EQU1## b) 4-(2,6-Dichloro-3-nitrobenzyloxy)benzothiazole
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834500 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-c67fcee6818b44f9bd1756eb14aa2056 |
| Source note | uspto-grants-1998_11 |