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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172356Generated: November 1, 2026

Cyclooctane → HCID 89500391, compound

https://huagongshe.com/reaction/2172356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclooctaneHCID 9266—
ReactantHCID 89500487HCID 89500487—
ProductHCID 89500391HCID 89500391—

Reaction Steps

6-cyclooctylidenehexanal is prepared according to the protocol described in Example 7 using cyclooctane in place of 2,4,4-trimethylcyclopentanone. The crude product containing cyclooctylidenehexanal is distilled under reduced pressure: its boiling point is 94° C. at 0.2 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051531B2
Source datasetuspto-grants-2015_06
ORD IDord-87738293fbe247d598461f49048eecb3
Source noteuspto-grants-2015_06