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US4117227A Expired / Lapsed US ⏱️ 0.0 years remaining

Production of n-(substituted) morpholine

Assignee: Texaco Development Corp
•
Filing: 1975-06-02
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Granted: 1978-09-26
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Expires: 1995-06-02
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Abstract

Abstract An improved process is disclosed for selectively producing an N-(substituted) morpholine compound from the corresponding N-(substituted) diethanolamine compound. The improved process includes contacting the N-(substituted) diethanolamine compound with a catalytically effective amount of a silica-alumina or certain phosphorus-containing substances at temperatures of from about 190° C to about 260° C under a pressure sufficient to maintain the mixture substantially in liquid phase and recovering from the reaction mixture the formed N-(substituted) morpholine. According to a preferred embodiment, triethanolamine is heated in the presence of a catalytically effective amount of a silica-alumina catalyst having an aluminum content of from about 5 to about 50 wt. % at temperatures of from about 240° C to about 260° C in liquid phase to selectively produce the corresponding N-(hydroxyethyl)morpholine (HEM).

Inventors

  • 👤 Michael E. Brennan

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 20:31
CPC Classifications
C; C07; C07D; C07D295/00; C07D295/04; C07D295/08; C07D295/084; C07D295/088; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/18; C08G18/20; C08G18/2009; C08G18/2018

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 100 words
A process for producing an N-(substituted) morpholine compound comprising the steps of contacting an alkanolamine of the formula: ##STR4## wherein R is an alkyl radical having from 1 to about 8 carbon atoms or a hydroxy alkyl radical having from 1 to about 10 carbon atoms and each R' is, independently, a hydrogen or a lower alkyl radical with a catalytically effective amount of ferric phosphate at a temperature of from about 190° C. to about 260° C. under a pressure sufficient to maintain the mixture substantially in liquid phase; and recovering said N-(substituted) morpholine compound from the reaction mixture.
Claim 2
Dependent Claim 100 words
A process for producing an N-(substituted) morpholine compound comprising the steps of contacting an alkanolamine of the formula: ##STR4## wherein R is an alkyl radical having from 1 to about 8 carbon atoms or a hydroxy alkyl radical having from 1 to about 10 carbon atoms and each R' is, independently, a hydrogen or a lower alkyl radical with a catalytically effective amount of ferric phosphate at a temperature of from about 190° C. to about 260° C. under a pressure sufficient to maintain the mixture substantially in liquid phase; and recovering said N-(substituted) morpholine compound from the reaction mixture.
Claim 3
Dependent Claim 111 words
A process for producing an N-(substituted) morpholine compound comprising the steps of contacting an alkanolamine of the formula: ##STR5## wherein R is an alkyl radical having from 1 to about 8 carbon atoms or a hydroxy alkyl radical having from 1 to about 10 carbon atoms and each R' is, independently, a hydrogen or a lower alkyl radical with a catalytically effective amount of phosphoric acid-impregnated silica having from about 10 to about 30 wt.% phosphoric acid at a temperature of from about 190° C. to about 260° C. under a pressure sufficient to maintain the mixture substantially in liquid phase; and recovering said N-(substituted) morpholine compound from the reaction mixture.
Claim 4
Dependent Claim 111 words
A process for producing an N-(substituted) morpholine compound comprising the steps of contacting an alkanolamine of the formula: ##STR5## wherein R is an alkyl radical having from 1 to about 8 carbon atoms or a hydroxy alkyl radical having from 1 to about 10 carbon atoms and each R' is, independently, a hydrogen or a lower alkyl radical with a catalytically effective amount of phosphoric acid-impregnated silica having from about 10 to about 30 wt.% phosphoric acid at a temperature of from about 190° C. to about 260° C. under a pressure sufficient to maintain the mixture substantially in liquid phase; and recovering said N-(substituted) morpholine compound from the reaction mixture.

References Cited (Backward Citations)

US615488A Cited
US3098072A Cited
US3654271A Cited
US3649627A Cited
US3641022A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-09-25 1982-03-27 1982-09-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-09-25 1986-03-27 1986-09-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-09-25 1990-03-27 1990-09-26 $7700.00 Window Closed / Lapsed

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