HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guaiacol → 4-(4'-Methylphenoxy)hexyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guaiacol | HCID 460 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,1-Dibromohexane | HCID 11806854 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(4'-Methylphenoxy)hexyl bromide | HCID 19023878 | 62% |
Reaction Steps
A solution of 62 g of methoxy phenol in 50 ml of methanol was added into a solution of 33.75 g of potassium hydroxide in 100 ml of methanol. The resulting solution was added dropwisely and slowly into 1 mole of α, -dibromohexane in 200 ml of acetone within 1 hour. After a reflux of the mixture for 1 hour, the mixture was concentrated and then diluted with water. The oil layer of the mixture was extracted with ethyl ether. Then, the ethyl ether layer was filtered and the filtrate was extracted with water. The solution was dried by calcium chloride, and 4-(4'-methoxyphenoxy) hexylbromide (compound 1, with a yield of 62%) was obtained by distillation under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05314976 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-b984902708d64c028391b2b44e7b8de3 |
| Source note | uspto-grants-1994_05 |