ES327698A2 - Procedure for the manufacture of alcanolamine derivatives. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the manufacture of alcanolamine derivatives. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES327698A2
ES327698A2 ES0327698A ES327698A ES327698A2 ES 327698 A2 ES327698 A2 ES 327698A2 ES 0327698 A ES0327698 A ES 0327698A ES 327698 A ES327698 A ES 327698A ES 327698 A2 ES327698 A2 ES 327698A2
Authority
ES
Spain
Prior art keywords
radical
carbon atoms
formula
alkyl
isopropyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES0327698A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of ES327698A2 publication Critical patent/ES327698A2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/24Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Materials For Medical Uses (AREA)
  • Tires In General (AREA)

Abstract

Improvements introduced in the object of the main patent No. 294,393, granted on February 18, 1964, by: "Procedure for the manufacture of alkanolamine derivatives", of the formula: ** (See formula) ** wherein R 1 represents a hydrogen atom or an alkyl radical of not more than 6 carbon atoms, such as methyl, ethyl or isopropyl, R 2 represents an alkyl, hydroxyalkyl radical of not more than 10 carbon atoms, such as a radical methyl, ethyl, n-propyl-isopropyl, s-butyl, t-butyl, 1-methyloctyl, or 2-hydroxy-1,1-dimethylethyl, or cycloalkyl of not more than 6 carbon atoms, such as a cyclopentyl radical and R3 represents an alkyl radical of 2 to 10 carbon atoms, such as an ethyl, isobutyl or n-heptyl radical, a haloalkyl radical of not more than 10 carbon atoms, such as a 2,2-dichloro-1 radical, 1-difluoroethyl, a cycloalkyl or alkenyl radical of not more than 6 carbon atoms, such as a cyclopentyl or allyl radical; and the aldehyde condensation products of those, of general formula ** (See formula) ** wherein R2 and R3 have the above-indicated meaning and R4 signifies hydrogen or an alkyl or aryl radical of not more than 10 carbon atoms, such as an isopropyl or phenyl radical and the aliphatic carboxylic esters of those of not more than 20 atoms carbon, such as acetic, palmitic, stearic or oleic, or aromatic carboxylic esters of not more than 10 carbon atoms, such as benzoic; and the salts thereof, such as hydrochlorides, hydrobromides, phosphates, sulfates, oxalates, lactates, tartrates, acetates, salicylates, citrates, benzoates, β -naphthoates, adipates, 1,1'-methylene-bis- (2- hydroxy-3-naphthoates) or salts derived from sulfonated polystene resins, characterized in that they comprise the interaction of a halogenated compound of the formula: ** (See formula) ** wherein Z represents a halogen atom such as chlorine or bromine and R3 has the meaning indicated above, with an amine of formula NHR1R2 in which R1 and R2 have the meaning indicated above. (Machine-translation by Google Translate, not legally binding)
ES0327698A 1965-06-08 1966-06-08 Procedure for the manufacture of alcanolamine derivatives. (Machine-translation by Google Translate, not legally binding) Expired ES327698A2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB24189/65A GB1128052A (en) 1965-06-08 1965-06-08 Alkanolamine derivatives

Publications (1)

Publication Number Publication Date
ES327698A2 true ES327698A2 (en) 1967-08-01

Family

ID=10207802

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0327698A Expired ES327698A2 (en) 1965-06-08 1966-06-08 Procedure for the manufacture of alcanolamine derivatives. (Machine-translation by Google Translate, not legally binding)

Country Status (9)

Country Link
US (1) US3538150A (en)
AT (1) AT282585B (en)
BE (1) BE682273A (en)
BR (1) BR6680266D0 (en)
DE (1) DE1543693A1 (en)
ES (1) ES327698A2 (en)
FI (1) FI45183B (en)
GB (1) GB1128052A (en)
NO (1) NO118172B (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE368197B (en) * 1968-11-18 1974-06-24 Pfizer
IT1113029B (en) * 1979-03-01 1986-01-20 Simes PROCESS FOR THE SEPARATION OF THE TWO OPTICAL ISOMERS OF MOPROLOL AND PHARMACEUTICAL COMPOSITIONS OF THE LEVOGIRO ANTIPOD
GB8327911D0 (en) * 1983-10-19 1983-11-23 Ciba Geigy Ag Salts as corrosion inhibitors
GB8419683D0 (en) * 1984-08-02 1984-09-05 Erba Farmitalia 3-substituted derivatives of 1-amino-2-hydroxy-propane
US5545412A (en) * 1985-01-07 1996-08-13 Syntex (U.S.A.) Inc. N-[1, (1-1)-dialkyloxy]-and N-[1, (1-1)-dialkenyloxy]-alk-1-yl-n,n,n-tetrasubstituted ammonium lipids and uses therefor
US4897355A (en) * 1985-01-07 1990-01-30 Syntex (U.S.A.) Inc. N[ω,(ω-1)-dialkyloxy]- and N-[ω,(ω-1)-dialkenyloxy]-alk-1-yl-N,N,N-tetrasubstituted ammonium lipids and uses therefor
ES8609190A1 (en) * 1985-02-07 1986-07-16 Pharma Investi S A A PROCEDURE FOR PREPARING PHENOLIC ETERS

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE583205A (en) * 1958-10-02
DE1236523C2 (en) * 1962-02-15 1975-06-12 Sanol-Arzneimittel Dr. Schwarz Gmbh, 4019 Monheim PROCESS FOR THE PRODUCTION OF BASIC PHENYLAETHERS AND THEIR SALTS
US3331850A (en) * 1964-05-13 1967-07-18 Upjohn Co 5-(aryloxymethyl)-2-oxazolidinethiones

Also Published As

Publication number Publication date
US3538150A (en) 1970-11-03
BE682273A (en) 1966-12-08
GB1128052A (en) 1968-09-25
AT282585B (en) 1970-07-10
FI45183B (en) 1971-12-31
NO118172B (en) 1969-11-24
DE1543693A1 (en) 1969-09-11
BR6680266D0 (en) 1973-12-26

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Legal Events

Date Code Title Description
FD2A Announcement of lapse in spain

Effective date: 20170629