HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2-(o-Tolylthio)-6-allylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(o-Tolylthio)phenol | HCID 15456664 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 2-(o-Tolylthio)-6-allylphenol | HCID 13066669 | 62.7% |
Reaction Steps
A mixture of 2-(o-tolylthio)phenol (32.7 g), allyl bromide (27.5 g) and dried potassium carbonate (42 g) in methyl isobutyl ketone (400 ml) was refluxed under heating for 4 hours. The reaction mixture was treated in the same manner as Example 21-(1) to give oily 2-(o-tolylthio)-6-allylphenol (24.3 g), bp. 150°-162° C./0.7-0.8 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367238 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-3e4edbe4c21f403b855ec63df725a467 |
| Source note | uspto-grants-1983_01 |