HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → HCID 22750662, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 70603592 | HCID 70603592 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 22750662 | HCID 22750662 | — |
Reaction Steps
13.5 g. of 1-methyl-5-(3-methylcarbethoxyaminopropyl)-5-hydroxy-5H-dibenzo[a,d]cycloheptene, 120 ml. of n-butanol and 14.5 g. of potassium hydroxide are boiled at reflux under an atmosphere of nitrogen for 20 hours. The solution is then evaporated to dryness and the residue taken up in ether. The ethereal solution is shaken out with dilute hydrochloric acid. The aqueous, acidic solution is again made alkaline with potassium carbonate. The oil which separates out is extracted with ether. The ethereal solution is washed with water, dried over sodium sulfate and evaporated. The 1-methyl-5-(3-methylaminopropyl)-5-hydroxy-5H-dibenzo[a,d]cycloheptene obtained is a thick oil which is immediately utilized as a reactant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04136116 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-cb57a854dfb840e4b34dbbd4a10ea5b4 |
| Source note | uspto-grants-1979_01 |