HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexane-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid | HCID 135583503 | — |
| Product | 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexane-carboxylic acid methyl ester | HCID 86740091 | — |
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 boiled together under reflux on a water separator for 18 hours. After cooling, the solution was washed with 500 ml. of a 5% sodium bicarbonate solution, then 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 ethylacetate, there was obtained 3-hydroxy-5-keto-4-phenylazo-3-cyclohexane-carboxylic acid methyl ester as a solid having a melting point of 144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515948 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-868bf62f9f3b4577a5c68b4a81b9ce0b |
| Source note | uspto-grants-1985_05 |