HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-Acetyl-beta-carboline-oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydroxylamine, N-chloro- | HCID 149953 | — |
| Reactant | 1-(9H-beta-Carbolin-3-yl)ethan-1-one | HCID 12789146 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Acetyl-beta-carboline-oxime | HCID 136399277 | 65.9% |
Reaction Steps
To a solution of 1.0 g of potassium hydroxide in 25 ml of methanol, there is added a mixture of 0.85 g of 3-acetyl-β-carboline, 75 ml of methanol and 1.0 g of hydroxyamino hydrochloride. The reaction mixture is allowed to stand for 4 hours at room temperature. After evaporation, water is added and then the mixture is brought to pH 7 with glacial acetic acid. The solid reaction product is filtered and washed with water and ether. 0.6 g of 3-acetyl-β-carboline-oxime with an m.p. of 250° C. (decomposition) is obtained. In analogous manner there is obtained: 3-pentanoyl-β-carboline-oxime, m.p. 95°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435403 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-19026031f8944776a9933a63ded3bb75 |
| Source note | uspto-grants-1984_03 |