PL442771A1 - Sposób otrzymywania azydku 2-dimetyaminoetylu - Google Patents

Sposób otrzymywania azydku 2-dimetyaminoetylu

Info

Publication number
PL442771A1
PL442771A1 PL442771A PL44277122A PL442771A1 PL 442771 A1 PL442771 A1 PL 442771A1 PL 442771 A PL442771 A PL 442771A PL 44277122 A PL44277122 A PL 44277122A PL 442771 A1 PL442771 A1 PL 442771A1
Authority
PL
Poland
Prior art keywords
sub
dimethylethylamine
hydrochloride
hydroxide
mol
Prior art date
Application number
PL442771A
Other languages
English (en)
Other versions
PL246993B1 (pl
Inventor
Wioleta Kopacz
Anna Kasztankiewicz
Grzegorz Rarata
Original Assignee
Sieć Badawcza Łukasiewicz-Instytut Lotnictwa
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 Sieć Badawcza Łukasiewicz-Instytut Lotnictwa filed Critical Sieć Badawcza Łukasiewicz-Instytut Lotnictwa
Priority to PL442771A priority Critical patent/PL246993B1/pl
Publication of PL442771A1 publication Critical patent/PL442771A1/pl
Publication of PL246993B1 publication Critical patent/PL246993B1/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/226Organic compounds containing nitrogen containing at least one nitrogen-to-nitrogen bond, e.g. azo compounds, azides, hydrazines
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B21/00Nitrogen; Compounds thereof
    • C01B21/08Hydrazoic acid; Azides; Halogen azides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L7/00Fuels produced by solidifying fluid fuels
    • C10L7/02Fuels produced by solidifying fluid fuels liquid fuels

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Przedmiotem zgłoszenia jest sposób otrzymywania azydku 2-dimetyaminoetylu, który polega na tym, że do chlorowodorku 2-chloro-N,N-dimetyloetyloaminy dodaje się wodę w ilości od 140 ml H<sub>2</sub>O/1 mol chlorowodorku 2-N,N-dimetyloetyloaminy do 280 ml H<sub>2</sub>O/1 mol chlorowodorku 2-N,N-dimetyloetyloaminy i po rozpuszczeniu substratu wprowadza się azydek sodu w ilości od 1,01:1 do 1,5:1 (mol/mol) w stosunku do ilości chlorowodorku 2-N,N-dimetyloetyloaminy. Mieszaninę reakcyjną podgrzewa się do temperatury 80 – 100°C i miesza pod chłodnicą zwrotną przez 10 minut — 2 godzin, a następnie produkt reakcji chłodzi się do temperatury pokojowej i powoli wkrapla wodny roztwór wodorotlenku nieorganicznego o stężeniu 25 - 40%, zawierającego od 0,9 ekwiwalentu wodorotlenku/1 ekwiwalent chlorowodorku 2-N,N-dimetyloetyloaminy do 1,55 ekwiwalentu wodorotlenku/1 ekwiwalent chlorowodorku 2-N,N-dimetyloetyloaminy. Po zakończeniu dozowania wodorotlenku układ miesza się jeszcze przez 15 do 90 minut, powstałe dwie fazy rozdziela się w rozdzielaczu a otrzymaną oleistą ciecz destyluje.
PL442771A 2022-11-09 2022-11-09 Sposób otrzymywania azydku 2-dimetyaminoetylu PL246993B1 (pl)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL442771A PL246993B1 (pl) 2022-11-09 2022-11-09 Sposób otrzymywania azydku 2-dimetyaminoetylu

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL442771A PL246993B1 (pl) 2022-11-09 2022-11-09 Sposób otrzymywania azydku 2-dimetyaminoetylu

Publications (2)

Publication Number Publication Date
PL442771A1 true PL442771A1 (pl) 2024-05-13
PL246993B1 PL246993B1 (pl) 2025-04-22

Family

ID=91070342

Family Applications (1)

Application Number Title Priority Date Filing Date
PL442771A PL246993B1 (pl) 2022-11-09 2022-11-09 Sposób otrzymywania azydku 2-dimetyaminoetylu

Country Status (1)

Country Link
PL (1) PL246993B1 (pl)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4499723A (en) * 1982-07-26 1985-02-19 Rockwell International Corporation Tris(2-azidoethyl)amine and method of preparation thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4499723A (en) * 1982-07-26 1985-02-19 Rockwell International Corporation Tris(2-azidoethyl)amine and method of preparation thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
GUNTER PAULUS SCHIEMENZ UND HERMANN ENGELHARD: "p.861, ex 6", TRIMETHOXYPHENYLVERBINDUNGEN, I, JUNI 1959"SYNTHESE VON AMINOAMIDEN UBER GEMISCHTE ANHYDRIDE", *
SHAHRAM G. PAKDEHI,* BAHMAN SHIRZADI: "2.1", EFFECT OF SOME INORGANIC NITRATE SALTS ON THE IGNITION DELAY TIME OF DMAZ-IRFNA AND DMAZ-WFNA BI-PROPELLANTS", CENT. EUR. J. ENERG. MATER. 2018, 15(1): 162-174 *

Also Published As

Publication number Publication date
PL246993B1 (pl) 2025-04-22

Similar Documents

Publication Publication Date Title
TW450963B (en) Acetamide derivative, process for preparing the same, and a pharmaceutical composition containing the same
TW502034B (en) 2-aryl-8-oxodihydropurine derivative, process for the preparation thereof, pharmaceutical composition containing the same, and intermediate therefor
CN115843272B (zh) Nek7激酶的抑制剂
CN101522641B (zh) 合成苯氧基二氨基嘧啶衍生物的方法
JPS63258880A (ja) 新規ピラゾロ〔3,4‐d〕ピリミジン、その製法並びにアレルギー性疾患、及び炎症により誘発される気管支痙攣性及び気管支収縮性反応を治療する医薬
CN103384641A (zh) 含氟磺酰亚胺盐的制造方法
BR112014020773A2 (pt) compostos de sulfonamida e seus usos como inibidores tnap
Schaider et al. Rosen & Barkin's 5-minute emergency medicine consult
US20160257667A1 (en) Synthesis of intermediates in the preparation of alk inhibitor
JP2022538491A (ja) ハイスループット化合物ライブラリー構築とスクリーニング方法および反応装置
CN115947717B (zh) 一类kif18a抑制剂
AU2025204788A1 (en) Nitrogen-containing heterocyclic pyridine compound
CA2859995A1 (en) Benzyl sulfonamide derivatives useful as mogat - 2 inhibitors
NO128569B (pl)
US20200031844A1 (en) Tetrahydrothiopyranopyrimidine derivatives as anti-HIV agent
TW587077B (en) Cyclic amide compound
TW201514153A (zh) 組蛋白去乙醯酶抑制劑及組成物,暨其使用之方法
CN110869371A (zh) 7-位取代吡咯并三嗪类化合物或其药学上可用的盐,及其制备方法和用途
PL442771A1 (pl) Sposób otrzymywania azydku 2-dimetyaminoetylu
CN114369085A (zh) 盐酸Asciminib的制备方法
CN103459392B (zh) 一种制备培美曲塞盐的方法
TW565559B (en) Sulfonamide-substituted chromans, processes for their preparation, their use as a medicament, and pharmaceutical preparations comprising them
Overberger et al. Monomer Synthesis. Methylation of 2-Aminopyrimidine1
AU2007338307A1 (en) Heterocyclyl-substituted-ehylamino-phenyl derivatives, their preparation and use as medicaments
CN104230787B (zh) N-(1,3-二氧代异吲哚啉)芳酰胺类化合物及其制备方法和应用