HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178442147, compound → HCID 178442329, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178442147 | HCID 178442147 | — |
| Reactant | HCID 178444359 | HCID 178444359 | — |
| Product | HCID 178442329 | HCID 178442329 | — |
Reaction Steps
30.4 g of 1-pentyl-4-(trans-4-pentylcyclohexyl)-cyclohexene [obtainable by reacting 4-(trans-4-pentylcyclohexyl)-cyclohexanone with pentyl-MgBr, hydrolysing the product to give 1-pentyl-4-(trans-4-pentylcyclohexyl)-cyclohexanol and dehydrating the latter], 2.7 g of liquid HCN, 0.1 g of palladium bis-[2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis-(diphenylphosphino)-butane] and 100 ml of acetonitrile are heated at 130° for 1 hour in an autoclave. The mixture is cooled, evaporated and worked up in the customary manner to give r-1-cyano-1-pentyl-cis-4-(trans-4-pentylcyclohexyl)-cyclohexane, m.p. 28°, c.p. 63°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510069 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-35607d48782148ca949c9fd6ac76162a |
| Source note | uspto-grants-1985_04 |