GB726260A - Quaternary amino compounds and processes for the production thereof - Google Patents

Quaternary amino compounds and processes for the production thereof

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Publication number
GB726260A
GB726260A GB12749/53A GB1274953A GB726260A GB 726260 A GB726260 A GB 726260A GB 12749/53 A GB12749/53 A GB 12749/53A GB 1274953 A GB1274953 A GB 1274953A GB 726260 A GB726260 A GB 726260A
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GB
United Kingdom
Prior art keywords
nc4h9
bis
phenyl
quaternary amino
amino compounds
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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
GB12749/53A
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Individual
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Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of GB726260A publication Critical patent/GB726260A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises quaternary amino compounds of the formula <FORM:0726260/IV (b)/1> in which R is an alkyl group of 1 to 3 carbon atoms, Z is the radical -CY=Y1C- or -CHY-CHY1-, where Y and Y1 are hydrogen or alkyl groups containing 1 to 6 carbon atoms, and Hal is a halogen. They are prepared by reacting the alkali metal phenolate of the 4,41-diphenol of the residue Z with 2 molecular equivalents of 2-dialkylamino-chloroethane to form the bis-(2-dialkylaminoethoxy-4-phenyl) derivative of Z, which is then quaternized with an alkyl halide. Examples describe the preparation of (1) the di-iodide of 1,2-bis-(4 - (2 - trimethylammonium - ethoxy) - phenyl)-pentene-1, and (2) the di-iodide of 1,2-bis-(4-(2-trimethylammonium - ethoxy) - phenyl) - pentane. Compounds also are described in which Z in the formula is -CH :CH-, -CH : C(CH3)-, -CH : C(C2H5)-, CH : C(iso C3H7)-, -CH : C(nC4H9)-, -C(C2H5) : C(C2H5)-(Cis and trans), -C(nC4H9) : C(nC4H9)-, C(nC6H13) : C(nC6H13)-, -CH2-CH2-, -CH2-CH(CH3)-, -CH2-CH(C2H5)-, -CH(C2H5)-CH(C2H5)-, -CH2-CH (iso C3H7)-, and -CH2-CH(nC4H9)-The 4,41-diphenol of the saturated residue Z may be prepared by catalytic hydrogenation of p the corresponding known unsaturated 4,41-dimethoxy derivatives followed by demethylation.
GB12749/53A 1952-05-07 1953-05-07 Quaternary amino compounds and processes for the production thereof Expired GB726260A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
BE726260X 1952-05-07

Publications (1)

Publication Number Publication Date
GB726260A true GB726260A (en) 1955-03-16

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Family Applications (1)

Application Number Title Priority Date Filing Date
GB12749/53A Expired GB726260A (en) 1952-05-07 1953-05-07 Quaternary amino compounds and processes for the production thereof

Country Status (1)

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GB (1) GB726260A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015163598A (en) * 2014-01-31 2015-09-10 株式会社デンソー Azobenzene compound and heat pump system using the same
WO2019209182A1 (en) * 2018-04-25 2019-10-31 Nanyang Technological University Conjugated oligoelectrolytes as antimicrobial agents
CN112154212A (en) * 2018-03-23 2020-12-29 加利福尼亚大学董事会 Short conjugated low polyelectrolyte and use thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015163598A (en) * 2014-01-31 2015-09-10 株式会社デンソー Azobenzene compound and heat pump system using the same
CN112154212A (en) * 2018-03-23 2020-12-29 加利福尼亚大学董事会 Short conjugated low polyelectrolyte and use thereof
US11713318B2 (en) 2018-03-23 2023-08-01 The Regents Of The University Of California Short conjugated oligoelectrolytes and uses thereof
WO2019209182A1 (en) * 2018-04-25 2019-10-31 Nanyang Technological University Conjugated oligoelectrolytes as antimicrobial agents
CN112313205A (en) * 2018-04-25 2021-02-02 南洋理工大学 Conjugated low polyelectrolytes as antibacterial agents
CN112313205B (en) * 2018-04-25 2023-12-26 南洋理工大学 Conjugated oligoelectrolytes as antibacterial agents

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