HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 23157338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 3-isopropoxy-4-methylbenzoate | HCID 23157412 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23157338 | HCID 23157338 | 64.6% |
Reaction Steps
To a solution of methyl 3-isopropoxy-4-methylbenzoate (1.0 g, 4.8 mmol) in ethyl acetate (20 mL) were added N-bromosuccinimide (0.92 g, 5.19 mmol) and 2,2′-azobis(isobutyronitrile) (3 mg), and the mixture was heated under reflux for 6 hr. The reaction mixture was allowed to cool, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-hexane/ethyl acetate=4/1) to give the title compound (0.89 g, yield 64%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786165B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-707677db8a334639a385383d4c13cd41 |
| Source note | uspto-grants-2010_08 |