HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 13505189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 13505188 | HCID 13505188 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13505189 | HCID 13505189 | 94.2% |
Reaction Steps
440 mg (1.31 mmol) of 6-(1-cyclohexen-4-yl)-4-methyl-β-carboline-3-carboxylic acid ethyl ester is heated under reflux for one hour in 20 ml of ethanol with 3.25 ml of 1N potassium hydroxide solution. After neutralizing with acetic acid and addition of 10 ml of water, the precipitated product is suctioned off, washed with water, and dried under vacuum over potassium hydroxide, thus obtaining 378 mg (94% of theory) of 6-(1-cyclohexen-4-yl)-4-methyl-β-carboline-3-carboxylic acid, mp 284°-285° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04623649 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-c40bd39e5f304e06876035e8c71181da |
| Source note | uspto-grants-1986_11 |