HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 372472Erstellt: 25. Oktober 2026
Methanol → 3(2,2-Dichlorovinyloxy)benzyl alcohol
https://huagongshe.com/reaction/372472
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium 4-methylbenzenesulfonate | HCID 3720192 | — |
| Edukt | 1-(Bromomethyl)-3-[(2,2-dichloroethenyl)oxy]benzene | HCID 20482706 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3(2,2-Dichlorovinyloxy)benzyl alcohol | HCID 53679295 | — |
Reaktionsschritte
A mixture of 3(2,2-dichlorovinyloxy)benzyl bromide (2.8 g), sodium p-toluene sulphonate (2.0 g) and methanol (20 ml) is warmed to 50° C for 1 hour, after which water (20 ml) and toluene (20 ml) is added with agitation. The toluene layer is separated, washed with water and concentrated by evaporation of the solvent under reduced pressure. The concentrate is then added dropwise to a 15% (w/v) aqueous solution of potassium hydroxide (100 ml) and the mixture warmed to 60° C for 1 hour, cooled to the ambient temperature and extracted with a mixture of toluene (10 ml) and methyl iso-butylketone (10 ml), the extracts dried over anhydrous magnesium sulphate and the solvents evaporated under reduced pressure to yield 3(2,2-dichlorovinyloxy)benzyl alcohol as a residual pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04091110 |
|---|
| Quelldatensatz | uspto-grants-1978_05 |
|---|
| ORD ID | ord-58d387cc901c460a9a7f8329d561f4d1 |
|---|
| Quellennotiz | uspto-grants-1978_05 |
|---|