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GB929378A - Nitroallyl alcohol esters - Google Patents

Nitroallyl alcohol esters

Info

Publication number
GB929378A
GB929378A GB621961A GB621961A GB929378A GB 929378 A GB929378 A GB 929378A GB 621961 A GB621961 A GB 621961A GB 621961 A GB621961 A GB 621961A GB 929378 A GB929378 A GB 929378A
Authority
GB
United Kingdom
Prior art keywords
nitroallyl
compounds
prepared
formula
alcohol esters
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
GB621961A
Inventor
Karl Klager
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.)
Aerojet Rocketdyne Inc
Original Assignee
Aerojet General Corp
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 Aerojet General Corp filed Critical Aerojet General Corp
Priority to GB621961A priority Critical patent/GB929378A/en
Publication of GB929378A publication Critical patent/GB929378A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises esters of nitroallyl alcohol having the formula:- <FORM:0929378/IV(a)/1> wherein R represents a C1-3 alkyl radical. The compounds are prepared by distilling a diester of 2-nitropropanediol having the formula:- <FORM:0929378/IV(a)/2> The above diester starting materials may be prepared in situ by condensing an appropriate acid halide or anhydride with 2-nitro1,3-propanediol. The above esters of nitroallyl alcohol react with compounds containing labile hydrogen, such as dinitroethane, to produce highly nitrated compounds, such as 2,2,4,6,6-pentanitroheptane.
GB621961A 1961-02-20 1961-02-20 Nitroallyl alcohol esters Expired GB929378A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB621961A GB929378A (en) 1961-02-20 1961-02-20 Nitroallyl alcohol esters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB621961A GB929378A (en) 1961-02-20 1961-02-20 Nitroallyl alcohol esters

Publications (1)

Publication Number Publication Date
GB929378A true GB929378A (en) 1963-06-19

Family

ID=9810580

Family Applications (1)

Application Number Title Priority Date Filing Date
GB621961A Expired GB929378A (en) 1961-02-20 1961-02-20 Nitroallyl alcohol esters

Country Status (1)

Country Link
GB (1) GB929378A (en)

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