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Process for the conversion of an alkane to a mixture of an alcohol and a ketone

Assignee: BP PLC
•
Filing: 1982-10-28
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Granted: —
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Expires: 2002-10-28
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Abstract

Abstract A mixture of the alcohol and ketone derivatives of alkanes is produced by reacting the alkane with a hydrocarbyl hydroperoxide, eg t-butyl hydroperoxide, at ambient or elevated temperature and pressure in the presence as catalyst of an iron or manganese square planar complex having heterocyclic nitrogen-donor ligands, eg a porphyrin or phthalocyanine complex, which complex has either no axial ligands, eg the lower valency or cationic complex, or an axial ligand which is non-coordinating or weakly-coordinating.

Inventors

  • 👤 Anthony Robert Middleton
  • 👤 David John Harry Smith

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-11-01 17:37
CPC Classifications
C; C07; C07C; C07C45/00; C07C45/27; C07C45/28; B; B01; B01J; B01J23/00; B01J23/16; B01J23/32; B01J23/34; B01J23/70; B01J23/74; B01J23/745; B01J31/00; B01J31/16; B01J31/18; B01J31/1805; B01J31/181; B01J31/1815; B01J31/1825; B01J31/183; C07C29/00; C07C29/132; C07C29/48; C07C31/00; C07C31/02; C07C31/12; C07C35/00; C07C35/02; C07C35/08; B01J2531/00; B01J2531/02; B01J2531/0238; B01J2531/0241; B01J2531/025; B01J2531/70; B01J2531/72; B01J2531/80; B01J2531/84; B01J2531/842; C07C2601/00; C07C2601/12; C07C2601/14

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 69 words
A process for the conversion of alkanes into a mixture of their corresponding alcohol and ketone derivatives which process comprises reacting the alkane with a hydrocarbyl hydroperoxide at ambient or elevated temperature and pressure in the presence as catalyst of an iron or manganese square planar complex having heterocyclic nitrogen donor ligands, which complex has either no axial ligand or an axial ligand which is non-coordinating or weakly coordinating.
Claim 2
Dependent Claim 69 words
A process for the conversion of alkanes into a mixture of their corresponding alcohol and ketone derivatives which process comprises reacting the alkane with a hydrocarbyl hydroperoxide at ambient or elevated temperature and pressure in the presence as catalyst of an iron or manganese square planar complex having heterocyclic nitrogen donor ligands, which complex has either no axial ligand or an axial ligand which is non-coordinating or weakly coordinating.
Claim 3
Dependent Claim 19 words
A process according to claim 1 wherein the alkane is a C 2 to C 10 linear or branched-alkane.
Claim 4
Dependent Claim 17 words
A process according to either one of the preceding claims wherein the hydrocarbyl hydroperoxide is t-butyl hydroperoxide.
Claim 5
Dependent Claim 20 words
A process according to any one of the preceding claims wherein the complex is a phthalocyanine or a porphyrin complex.
Claim 6
Dependent Claim 26 words
A process according to any one of the preceding claims wherein the complex has no axial ligands and is an iron (11) or manganese (11) complex.
Claim 7
Dependent Claim 28 words
A process according to claim 5 wherein the iron (11) or manganese (11) complex is obtained by chemical reduction of the corresponding iron (111) or manganese (111) complex.
Claim 8
Dependent Claim 28 words
A process according to any one of claims 1 to 5 wherein the complex has no axial ligands and is an iron (111) or manganese (III) cationic complex.
Claim 9
Dependent Claim 21 words
A process according to claim 7 wherein the cation moiety of the cationic complex is [Fe(lll)(TPP)] + or [Mn(lll)(TPP)] + .
Claim 10
Dependent Claim 33 words
A process according to claim 8 wherein the cationic complex is prepared by reacting Fe(III)(TPP)Cl or Mn(lll)(TPP)Cl with a silver salt of phosphorus hexafluoride, phosphorus hexachloride, antimony hexafluoride, antimony hexachloride, tetraphenylboron or tetrafluoroboron.
Claim 11
Dependent Claim 22 words
A process according to any one of claims 1 to 5 wherein the complex has a non-coordinating or weakly coordinating axial ligand.
Claim 12
Dependent Claim 37 words
A process according to claim 10 wherein the complex is formed 'in-situ' from a complex having a strongly coordinating axial ligand by the addition of an acid which is either sulphuric acid, boric acid or benzoic acid.

References Cited (Backward Citations)

US3816548A Cited
SU825480A1 Cited
EP0027937A1 Cited

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