HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2-(2-Chlorophenylthio)-6-allylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2-Chlorophenylthio)phenol | HCID 20513469 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 2-(2-Chlorophenylthio)-6-allylphenol | HCID 13066668 | 83.5% |
Reaction Steps
A mixture of 2-(2-chlorophenylthio)phenol (33 g), allyl bromide (25 g) and dried potassium carbonate (29 g) in methyl isobutyl ketone (200 ml) was refluxed under heating for 1.5 hours. After cooling to the ambient temperature, the reaction mixture was filtered, and the filtrate was evaporated under reduced pressure. The resultant oily residue was stirred at 230° C. for 3 hours and then distilled under reduced pressure to give oily 2-(2-chlorophenylthio)-6-allylphenol (32.2 g) bp 157°-162° C./0.7 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367238 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-e1215f4f06b9471583ca78ed7edf3cc8 |
| Source note | uspto-grants-1983_01 |