HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzoic Acid → 3-Cyclohexene-1-carboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzoic Acid | HCID 243 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Produkt | 3-Cyclohexene-1-carboxylic acid | HCID 20903 | — |
| Produkt | 3-Cyclohexene-1-carbonyl chloride | HCID 523058 | — |
Reaktionsschritte
The 4-hydroxy group of 4-hydroxybenzoic acid is protected by reacting 4-hydroxybenzoic acid, 5 g (0.036 mol), obtained commercially, with benzyl chloride, 5.1 g (0.04 mol) in ethanol:water (1:1) containing 5 g K2CO3 (0.04 mol) at a temperature of 30 degrees C. for 12 hours. The 4-PgO benzoic acid is converted to the acid chloride using thionyl chloride by a procedure similar to that employed for producing 3-cyclohexene carboxylic acid chloride from 3-cyclohexene carboxylic acid in Example I.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05948922 |
| Quelldatensatz | uspto-grants-1999_09 |
| ORD ID | ord-7437a50ac67e4cc1b705e829f4cfc34c |
| Quellennotiz | uspto-grants-1999_09 |