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US3965187A Expired / Lapsed US ⏱️ 0.0 years remaining

Hydrogenation of phenol

Assignee: Honeywell International Inc
•
Filing: 1970-07-02
•
Granted: 1976-06-22
•
Expires: 1990-07-02
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Abstract

Abstract The catalytic hydrogenation of phenol obtained by the cumene hydroperoxide process is improved by hydrogenating high purity phenol containing not more than 75 ppm of acetol, an impurity found in phenol prepared from cumene. Acetol-free phenol is obtained by treating phenol for 1-5 minutes with a polyamine such as hexamethylene diamine, hexamethylene triamine and the like or an aqueous solution thereof, and then distilling the mixture to separate the components. Alternatively, the hydrogenability of phenol can be improved by injecting the polyamine into the reaction mixture during hydrogenation.

Inventors

  • 👤 Edwin D. Little
  • 👤 Zafarullah K. Cheema

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 23:21
CPC Classifications
C; C07; C07C; C07C45/00; C07C45/006

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 161 words
In the process for hydrogenating phenol in the presence of hydrogenation catalyst in liquid or vapor phase at temperature of 24° to 400°C., using as starting material phenol having a purity of at least 99.8 percent obtained from fractional distillation of the cumene hydroperoxide decomposition product containing acetol as an impurity, the improvement which comprises: treating said phenol by contact with a polyamine of the formula: ##EQU4## wherein n is an integer from 0 to 4; R 1 , R 2 and R 3 are independently selected from the group consisting of hydrogen, alkyl, aryl, cycloalkyl, aralkyl and alkaryl and R independently at each occurrence is selected from the group of radicals consisting of alkylene, arylene, alkylenearylene, dialkylene, cycloaklyene, dialkylene cycloalkylene, nitrogen containing heterocyclic groups of 5 to 6 carbon atoms, and the lower alkyl substituted, hydroxy substituted and carboxyl substituted derivatives of said radicals to reduce its acetol content to a level of less than 75 ppm prior to hydrogenation.
Claim 2
Dependent Claim 161 words
In the process for hydrogenating phenol in the presence of hydrogenation catalyst in liquid or vapor phase at temperature of 24° to 400°C., using as starting material phenol having a purity of at least 99.8 percent obtained from fractional distillation of the cumene hydroperoxide decomposition product containing acetol as an impurity, the improvement which comprises: treating said phenol by contact with a polyamine of the formula: ##EQU4## wherein n is an integer from 0 to 4; R 1 , R 2 and R 3 are independently selected from the group consisting of hydrogen, alkyl, aryl, cycloalkyl, aralkyl and alkaryl and R independently at each occurrence is selected from the group of radicals consisting of alkylene, arylene, alkylenearylene, dialkylene, cycloaklyene, dialkylene cycloalkylene, nitrogen containing heterocyclic groups of 5 to 6 carbon atoms, and the lower alkyl substituted, hydroxy substituted and carboxyl substituted derivatives of said radicals to reduce its acetol content to a level of less than 75 ppm prior to hydrogenation.
Claim 3
Dependent Claim 30 words
The improvement of claim 1 wherein the phenol is treated with 0.01 to 2 percent by weight of said polyamine compound and is distilled to separate the polyamine and acetol.
Claim 4
Dependent Claim 21 words
The improvement of claim 2 wherein the phenol is treated with said polyamine compound at a temperature of 40° to 220°C.
Claim 5
Dependent Claim 12 words
The method of claim 1 wherein the polyamine compound is hexamethylene diamine.
Claim 6
Dependent Claim 12 words
The method of claim 1 wherein the polyamine compound is hexamethylene triamine.

References Cited (Backward Citations)

US2737480A Cited
US2886601A Cited
US3029294A Cited
US3076810A Cited
US3187050A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-06-22 1979-12-22 1980-06-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-06-22 1983-12-22 1984-06-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-06-22 1987-12-22 1988-06-22 $7700.00 Window Closed / Lapsed

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