HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromo-5,5-dimethylhydantoin → HCID 22008912, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 22008918 | HCID 22008918 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 22008912 | HCID 22008912 | 181.8% |
Reaction Steps
A mixture of 5.8 g (20.0 mmol) of 1,3-dibromo-5,5-dimethylhydantoin and 0.5 g of azobisisobutyronitrile was added in portions at 110° C. to a solution of 8.0 g (40.0 mmol) of 2-methoxy-6-chloro-3-nitrotoluene from Example 11aα) in 50 ml of chlorobenzene. After 1 h, a mixture of 3.0 g (10 mmol) of 1,3-dibromo-5,5-dimethylhydantoin and 0.2 g of azobisisobutyronitrile was again added. After a further 1.5 h, the mixture was allowed to cool, and 500 ml of ethyl acetate were added to the reaction solution. The resulting mixture was washed once each with satd Na2SO3 solution, Na2CO3 solution, and NaCl solution, dried (MgSO4), and concentrated. 10.2 g of the title compound resulted in the form of an amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211196B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-f5d466a23c8246e68a0b4120079f8ab1 |
| Source note | uspto-grants-2001_04 |