HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → HCID 178442036, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Reactant | HCID 178442037 | HCID 178442037 | — |
| Reactant | HCID 178442038 | HCID 178442038 | — |
| Solvent | Triethylene Glycol | HCID 8172 | — |
| Product | HCID 178442036 | HCID 178442036 | — |
Reaction Steps
A mixture of 3.2 g of 1-n-pentyl-4-(trans-4-propionylcyclohexyl)-bicyclo[2.2.2]octane [obtainable by reacting 1-n-pentyl-4-(trans-4-cyanocyclohexyl)-bicyclo[2.2.2]octane (German Offenlegungsschrift Pat. No. 3,246,440) with C2H5MgBr and hydrolysing the product], 3 g of KOH, 5 ml of 85% hydrazine and 50 ml of triethylene glycol is heated at 120° C. for 1 hour. The temperature is increased slowly until the resulting hydrazone is decomposed, and the mixture is boiled for a further 4 hours, cooled and worked up in the customary manner to give 1-n-pentyl-4-(trans-4-n-propylcyclohexyl)-bicyclo[2.2.2]octane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04707295 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-8a7dc2be881f4896932102ba9cf17d3c |
| Source note | uspto-grants-1987_11 |