HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 13750614, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-Isopropenylphenol | HCID 584247 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13750614 | HCID 13750614 | 63% |
Reaction Steps
A 10 g-portion of p-isopropenylphenol, 1.0 equivalent allyl bromide, 1.0 equivalent K2CO3, and 20 ml acetone were mixed and refluxed overnight. The reaction mixture was poured into 60 ml water and extracted with two portions of ether. The combined ether layers were washed with two portions of 10% aqueous NaOH, two portions of saturated aqueous NaCl and dried over K2CO3. Removal of solvent followed by distillation under reduced pressure gave a 63% yield of 1-(1-methylethenyl)-4-(2-propenyloxy)benzene, mp 22°-23° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04691042 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-0d5794a1b57b46e484a7d71f6af50c18 |
| Source note | uspto-grants-1987_09 |