HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Benzene, 1,2-dichloro-3-(2-propenyloxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 2,3-Dichlorophenol | HCID 11334 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzene, 1,2-dichloro-3-(2-propenyloxy)- | HCID 637359 | — |
Reaction Steps
A mixture of 2,3-dichlorophenol (35.5 g., 0.22 mole), allyl bromide (29.4 g., 0.24 mole) and potassium carbonate (33 g., 0.24 mole) in dimethylformamide (200 ml.) is vigorously stirred and heated at 55°-60° C. for one hour, poured into ice water, extracted with ether, washed with water and dried over magnesium sulfate. Evaporation of the ether leaves 2,3-dichlorophenyl allyl ether which is subjected to a Claisen rearrangement by heating at 250° C. for ten minutes. Distillation gives 36 g. of 2,3-dichloro-6-allylphenol which boils at 132°-4°/13 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04181727 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-7ad2ec4bfe5a4e87b1347bb15e42dfd5 |
| Source note | uspto-grants-1980_01 |