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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030019Generated: October 26, 2026

Benzene → Benzaldehyde

https://huagongshe.com/reaction/1030019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantIsopropanolHCID 3776—
ReactantCyclooctaneHCID 9266—
ReactantHCID 178418361HCID 178418361—
ProductBenzaldehydeHCID 240—
ProductBenzyl AlcoholHCID 244—
ProductBiphenylHCID 7095—

Reaction Steps

The experimental procedure was substantially the same as in Example 1 except that the amount of benzene as the starting hydrocarbon compound was decreased to 12 ml while 13.8 ml of isopropyl alcohol were replaced with 18 ml of cyclooctane as the hydrogen donor compound. The result of the analysis of the reaction mixture after completion of the reaction was that the molar yields of benzyl alcohol, benzaldehyde and biphenyl were 6624%, 350% and 8%, respectively, based on the molar amount of the rhodium complex used as the catalyst. Small amounts of cyclooctane carbaldehyde and cyclooctanemethanol were detected in the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104504
Source datasetuspto-grants-1992_04
ORD IDord-3b78011df78045d6b31e32042433843d
Source noteuspto-grants-1992_04