HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylphenol → 1-(Allyloxy)-4-tert-butylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-(Allyloxy)-4-tert-butylbenzene | HCID 600124 | — |
Reaction Steps
A mixture of 45 g 4-(1,1-dimethylethyl)phenol, 30 g 3-chloro-1-propene, 50 g anhydrous potassium carbonate and 250 ml 2-butanone was refluxed for 15 hours, after which time the solvent was removed in a rotary evaporator. Water was added to dissolve the potassium salts and the product extracted twice with ether. The ether layer was dried, removed, and the product distilled. The 50 grams of 1-(1,1-dimethylethyl)-4-(2-propenyloxy)benzene was found to boil at 70°-75° C. at 0.2 mm Hg, listed in Table 1 as compound I-4)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05486533 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-a451815d4b3a4939b1c7aca8fb4fc062 |
| Source note | uspto-grants-1996_01 |