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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704304Generated: October 30, 2026

HCID 178442147, compound → HCID 178442329, compound

https://huagongshe.com/reaction/704304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178442147HCID 178442147—
ReactantHCID 178444359HCID 178444359—
ProductHCID 178442329HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04986931
Source datasetuspto-grants-1991_01
ORD IDord-70209668e55f4f66b515377cd30b6fc7
Source noteuspto-grants-1991_01