HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guaiacol → HCID 10967048, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guaiacol | HCID 460 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Diallyl ether | HCID 11194 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methoxy-6-(prop-2-en-1-yl)phenol | HCID 347577 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Mesitylene | HCID 7947 | — |
| Product | HCID 10967048 | HCID 10967048 | 45% |
Reaction Steps
Treatment of guaiacol (25.00 g, 0.201 mol) with allyl bromide (29.24 g, 0.242 mol) and potassium carbonate (83.50 g, 0.604 mol) followed by refluxing the resultant allyl ether in mesitylene generally according to the procedure described for Intermediate 8 afforded 2-allyl-6-methoxyphenol as a brown oil. Treatment of the phenol with potassium carbonate (83.5 g, 0.604 mol), benzyl bromide (36.19 g, 0.212 mol), and tetrabutylammonium iodide (7.42 g, 0.020 mol) generally according to the procedure described for Intermediate 1 gave 23.61 g (45%) of 1-allyl-2-(benzyloxy)-3-methoxybenzene as a pale yellow oil. Rf=0.71 (silica, ethyl acetate:hexanes 1:9); Anal. calcd. for C17H18O2: C, 80.28; H, 7.13. Found: C, 79.09; H, 6.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435837B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-2635616f4f0c46fb922d7ccf270fe0c7 |
| Source note | uspto-grants-2008_10 |