HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371166Generated: November 1, 2026
Hydrochloric Acid → HCID 20274349, compound
https://huagongshe.com/reaction/371166
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 20274363 | HCID 20274363 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20274349 | HCID 20274349 | — |
Reaction Steps
A mixture of 2.32 g (5 mmoles) of N-isobutyl-2-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-piperidone, 10.2 ml hydrazine hydrate and 20 ml ethylene glycol is heated at 100° C. for one hour. The mixture is cooled to 60° C, and 4.05 g (72.3 mmoles) solid potassium hydroxide is added. After heating at 200° C. for two hours, the reaction mixture is cooled and added to 500 ml 1N hydrochloric acid and 300 ml ethyl ether. The ether layer is separated, washed with brine, sodium bicarbonate solution, dried over magnesium sulfate and the solvent evaporated at reduced pressure. The crude product is purified, if desired, by column chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04529732 |
|---|
| Source dataset | uspto-grants-1985_07 |
|---|
| ORD ID | ord-f9d1949934ec48ddb0ed3ca63235752b |
|---|
| Source note | uspto-grants-1985_07 |
|---|