HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 12531835 | HCID 12531835 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 20392594 | — |
Reaction Steps
To a solution of 1.38 g of methyl α-[p-(p-chlorophenoxy)phenyl]acetate in 15 ml of carbon tetrachloride is added 0.92 g of N-bromosuccinimide and a small drop of concentrated HBr. The mixture is maintained at reflux for 72 hours and cooled to room temperature. Filtration through 50 g of aluminum oxide, evaporation of the solvent and bulb-to-bulb distillation of the residue (166° @ 0.05 mm) affords the product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168385 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-d892a64dd6bb42f0aa12b3a5597b66a8 |
| Source note | uspto-grants-1979_09 |