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 AlBN (5 g) was added in portions at 150° C. to 2,6-dichloro-3-nitrotoluene (100 g, 0.48 mol) in chlorobenzene (400 ml). After 1 h, a mixture of dibromohydantoin (35 g, 0.12 mol) and AIBN (2.5 g) was again added. After a further 1.5 h, the mixture was allowed to cool and EA (500 ml) was added. This mixture was washed once each with saturated Na2SO3, Na2CO3 and NaCl solution, dried (MgSO4) and concentrated, the title compound being obtained as an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859025 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-b7a568ba3d00424294d137ce07854653 |
| Source note | uspto-grants-1999_01 |