HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-(Bromomethyl)-5-methyl-1,3-dioxol-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4,5-Dimethyl-1,3-dioxol-2-one | HCID 142210 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(Bromomethyl)-5-methyl-1,3-dioxol-2-one | HCID 10774141 | 112.3% |
Reaction Steps
Combine 4,5-dimethyl-1,3-dioxol-2-one (3.42 g, 30 mmol), N-bromosuccinimide (5.34 g, 30 mmol) and AIBN (500 mg, 3 mmol) in anhydrous carbon tetrachloride (100 mL). Heat at reflux. After 2 hours, cool and filter. Concentrate the filtrate to give 4-bromomethyl-5-methyl-1,3-dioxol-2-one (6.5 g, crude) as an oil, which can be used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977139 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-4a4501c9981543c0ae844cfdfd3cfbf1 |
| Source note | uspto-grants-1999_11 |