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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578665Generated: November 4, 2026

Ethanol → 1-Hexanol

https://huagongshe.com/reaction/1578665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-PenteneHCID 8004—
ReactantTriphenylphosphineHCID 11776—
ReactantRhodium chlorideHCID 24872—
ReactantChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventBenzeneHCID 241—
Product1-HexanolHCID 8103—
Product4-Methyl-1-pentanolHCID 12296—
ProductChlorotris(triphenylphosphine)rhodium(I)HCID 84599—

Reaction Steps

Chlorotris(triphenylphosphine)rhodium(I), [(03P)3RhCl], was prepared by refluxing an ethanol solution of rhodium(III) chloride in the presence of an excess amount of triphenylphosphine. Chlorotris(triphenylphosphine)rhodium(I) was dissolved in benzene, and the microspheres of Example III were added to the resulting red solution in an autoclave, equipped with a magnetic driven stirrer. Pentene-1 was introduced to the reactor along with benzene. The reaction was performed under conditions similar to Example IV. About 82% of the feed was reacted to give predominantly isohexanol and n-hexanol. The solid catalyst left inside of the reactor from this run was rinsed with fresh portions of benzene, and saved for another run.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03937742
Source datasetuspto-grants-1976_02
ORD IDord-a139d5fb50024904a4df2e9a278658fa
Source noteuspto-grants-1976_02