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US3715404A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for selective hydrogenation

Assignee: F Hoffmann La Roche AG
•
Filing: 1968-09-19
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Granted: 1973-02-06
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Expires: 1988-09-19
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Abstract

Abstract A process for selective hydrogenation of unsaturated organic compounds having at least four carbon atoms by carrying out said hydrogenation in a liquid phase in the presence of an organic sulfur compound utilizing a partially deactivated palladium catalyst.

Inventors

  • 👤 H Lindlar
  • 👤 R Dubuis

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 09:19
CPC Classifications
B; B01; B01J; B01J37/00; B01J37/20; B01J23/00; B01J23/38; B01J23/40; B01J23/44; C; C07; C07C; C07C29/00; C07C29/17

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 180 words
A process for the hydrogenation of organic compounds selected from the group consisting of aliphatic hydrocarbons containing from four to 45 carbon atoms and having one or more triple bonds, aryl and cycloalkyl hydrocarbons containing from eight to 45 carbon atoms and having an aliphatic side chain with one or more triple bonds, hydroxy substituted aliphatic hydrocarbons containing from four to 45 carbon atoms and one or more triple bonds, cycloalkyl hydrocarbons containing from eight To 45 carbon atoms having a hydroxy substituted aliphatic side chain with one or more triple bonds, carboxy substituted aliphatic hydrocarbons containing from four to 45 carbon atoms and having one or more triple bonds and aryl containing hydrocarbons containing six to 45 carbon atoms and at least one keto group directly attached to the aryl moiety comprising hydrogenating said organic compound in a liquid medium in the presence of a palladium catalyst partially deactivated with lead, bismuth, copper, zinc, tin mercury, cadmium or thorium; and a sulfur derivative of the formula: HO-(CH2) x-S-(CH2)x-S-(CH2)x-OH wherein x is an integer of from 1 to 6 inclusive.
Claim 2
Dependent Claim 180 words
A process for the hydrogenation of organic compounds selected from the group consisting of aliphatic hydrocarbons containing from four to 45 carbon atoms and having one or more triple bonds, aryl and cycloalkyl hydrocarbons containing from eight to 45 carbon atoms and having an aliphatic side chain with one or more triple bonds, hydroxy substituted aliphatic hydrocarbons containing from four to 45 carbon atoms and one or more triple bonds, cycloalkyl hydrocarbons containing from eight To 45 carbon atoms having a hydroxy substituted aliphatic side chain with one or more triple bonds, carboxy substituted aliphatic hydrocarbons containing from four to 45 carbon atoms and having one or more triple bonds and aryl containing hydrocarbons containing six to 45 carbon atoms and at least one keto group directly attached to the aryl moiety comprising hydrogenating said organic compound in a liquid medium in the presence of a palladium catalyst partially deactivated with lead, bismuth, copper, zinc, tin mercury, cadmium or thorium; and a sulfur derivative of the formula: HO-(CH2) x-S-(CH2)x-S-(CH2)x-OH wherein x is an integer of from 1 to 6 inclusive.
Claim 3
Dependent Claim 14 words
The process of claim 1 wherein said palladium catalyst is partially deactivated with lead.
Claim 4
Dependent Claim 25 words
The process of claim 1 wherein at least 0.1 percent by weight of said sulfur derivative, based on the weight of said catalyst, is used.
Claim 5
Dependent Claim 11 words
The process of claim 1 wherein said sulfur derivative is 1,2-bis-(2-hydroxyethylthio)-ethane.
Claim 6
Dependent Claim 14 words
The process of claim 1 wherein said organic compound is a hydroxy substituted hydrocarbon.
Claim 7
Dependent Claim 11 words
The process of claim 5 wherein said organic compound is 3-methyl-butyn-(1)-ol-(3).
Claim 8
Dependent Claim 14 words
The process of claim 5 wherein said palladium catalyst is partially deactivated with lead.

References Cited (Backward Citations)

DE288271C Cited
US2300598A Cited
US2681938A Cited
US2992278A Cited
US3075024A Cited
US3336239A Cited
US3450776A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1976-02-06 1976-08-07 1977-02-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1980-02-06 1980-08-07 1981-02-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1984-02-06 1984-08-07 1985-02-06 $7700.00 Window Closed / Lapsed

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