HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid | HCID 135583503 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid methyl ester | HCID 136056374 | — |
Reaction Steps
60 G. of 3-hydroxy-5-keto-4-phenylazo-3-cyclohexene-carboxylic acid, 200 ml. of methanol, 1200 ml. of benzene and 5 g. of p-toluenesulfonic acid were heated together at reflux for 18 hours on a water separator. After cooling, the solution was washed with 500 ml. of a 5% sodium bicarbonate solution, washed with water, dried and evaporated. The residue was dissolved in ethyl acetate and purified on an aluminum oxide column (500 g., activity stage I). After evaporation of the ethyl acetate, there was obtained 3-hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid methyl ester of melting point 144° C. (from benzene/petroleum ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024145 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-c0a53e7041de484e8468513e11c4954d |
| Source note | uspto-grants-1977_05 |