Azobisisobutyronitrile → 4-(Bromomethyl)-5-methyl-1,3-dioxol-2-one

HRID 2166829Notes

Reaction equation

HRID 2166829 reaction equation
[CH3:1][C:2]1[O:3][C:4](=[O:8])[O:5][C:6]=1[CH3:7].[Br:9]N1C(=O)CCC1=O.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:9][CH2:1][C:2]1[O:3][C:4](=[O:8])[O:5][C:6]=1[CH3:7]

Participants

5

Procedure

In 150 ml of carbon tetrachloride was dissolved 3.42 g of 4,5-dimethyl-1,3-dioxolen-2-one (synthesized by the method described in Tetrahedron Letters, 1972 pages 1701-1704). N-bromosuccinimide (5.34 g) and a catalytic amount of α,α'-azobisisobutyronitrile were added to the solution, and the mixture was heated under reflux for 15 minutes. The reaction mixture was concentrated to one half of its volume, and the insoluble material was removed by filtration. The filtrate was concentrated, and the syrupy residue was distilled under reduced pressure to give 4.2 g (yield 73%) of a colorless liquid having a boiling point of 115°-120° C./5 mm. The product had the following properties.

Workup

  1. customsynthesized by the method
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for 15 minutes
  4. concentrationThe reaction mixture was concentrated to one half of its volume
  5. customthe insoluble material was removed by filtration
  6. concentrationThe filtrate was concentrated
  7. distillationthe syrupy residue was distilled under reduced pressure

Sources & evidence

ORD record
ord-2fce71d4db8e4e86bf51dcc6ab8abcaf
Source dataset
uspto-grants-1983_06
Patent number
US04389408

Reaction notes

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