HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Formaldehyde → Benzyl 4-hydroxy-3-hydroxymethylbenzoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Propionic Acid | HCID 1032 | — |
| Edukt | Benzyl 4-Hydroxybenzoate | HCID 7180 | — |
| Edukt | Phenylboronic Acid | HCID 66827 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Benzyl 4-hydroxy-3-hydroxymethylbenzoate | HCID 19372223 | 287,2% |
Reaktionsschritte
A solution of 27.4 g (0.12 mole) of benzyl 4-hydroxybenzoate, 14.7 g (0.12 mole) of benzeneboronic acid, 6 g (0.135 mole) of paraformaldehyde and 0.9 ml (12 mmoles) of propionic acid in 600 ml of anhydrous benzene is heated at reflux for 12 hours using a Dean-Stark reactor to separate the water formed. The reaction medium is poured into bicarbonated water and extracted with ethyl ether. The organic phase is decanted, washed with water, dried on magnesium sulfate and evaporated. The resulting residue is purified by chromatography on a silica column eluted with dichloromethane. After evaporation of the solvent, 8.9 g (30% yield) of the expected product having a melting point of 109°-110° C. are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05468897 |
| Quelldatensatz | uspto-grants-1995_11 |
| ORD ID | ord-fc764d4caba24ff4bb41abc4b7299f25 |
| Quellennotiz | uspto-grants-1995_11 |