CS202897B1 - 1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof - Google Patents

1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof Download PDF

Info

Publication number
CS202897B1
CS202897B1 CS43379A CS43379A CS202897B1 CS 202897 B1 CS202897 B1 CS 202897B1 CS 43379 A CS43379 A CS 43379A CS 43379 A CS43379 A CS 43379A CS 202897 B1 CS202897 B1 CS 202897B1
Authority
CS
Czechoslovakia
Prior art keywords
phenyl
hydroxyethoxy
preparing
ethandione
formula
Prior art date
Application number
CS43379A
Other languages
English (en)
Slovak (sk)
Inventor
Ivan Zvara
Ivan Lukac
Pavol Hrdlovic
Original Assignee
Ivan Zvara
Ivan Lukac
Pavol Hrdlovic
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 Ivan Zvara, Ivan Lukac, Pavol Hrdlovic filed Critical Ivan Zvara
Priority to CS43379A priority Critical patent/CS202897B1/cs
Publication of CS202897B1 publication Critical patent/CS202897B1/cs

Links

Landscapes

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

Description

Vynález sa týká novej zlúčeniny 1-fenyl-2-[-4/2-hydroxyetoxy/fenyl}-1 ,2-etándiónu vzorca I co-co
CHj—CHj—OH /1/ a sposobu jej přípravy.
Spčsob přípravy novej zlúčeniny, ktorá je známa z literatúry, je založený na tom, že 1-hydroxy-2-^/4-fenyl-acetyl/-fenoxyJ-etán vzorca II (2^-CH2-CO-^O^-O-CH2- ch2-oh /11/ sa oxiduje kysličníkom seleničitým v prostředí vodného dioxánu pri refluxe.
Uvedená zlúčenina je medziprodukt syntézy polyméru so špeciálnym používáním.
Příklad mól 1-hydroxy-2-f/4-fenylacety 1/fenoxyJ-etánu sa rozpustí v dioxáne a přidá sa k němu roztok 1,1 molu kyslíčníka seleničitého, 1^1 molu vody v dioxáne a zmes sa refluxuje 5 až 8 hodin. Po tomto čase sa reakčná zmes přefiltruje, dioxán sa vákuovo odpaří a produkt sa krystalizuje z etanolu. Získá sa žitá krystalická látka o t.t. 104,5-105,5,°C a výtažok je 42Z. Hmotnostně spektrum M/e = 270, 166, 120, 105, 93, 76, 45 1 H NMR /CDC13/ delta = 2,67 /s, 1H/0H/; 4,43/ m, 4H/~O-CH2-CH2~O-//; 7,83 /m, 9H arom./ elementárna analýza vyp. C = 71,10 Z zistené C = 71,17 Z B = 5,22.2 H - 5,3 1 Z '

Claims (2)

  1. PREDMET VYNÁLEZU
    1. 1-feny1-2-£-4/2-hydroxyetoxy/fenyl]-1,2-etándíón vzorca I <^O)-COrCO-<^Oj>-O-CH2-CH2-OH
  2. 2. Sposob přípravy novej zlúčeniny podía bodu 1, vyznačujúci sa tým, že 1-hydroxy-2 C/4-f enylacety 1/fenoxy]-etán vzorca IX ‘ <Qhch2-co-^o^-o-ch2-ch2-oh /11/ sa oxiduje kysličníkom seleničitýmv prostředí vodného dioxánu pri refluxe.
CS43379A 1979-01-19 1979-01-19 1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof CS202897B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CS43379A CS202897B1 (en) 1979-01-19 1979-01-19 1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CS43379A CS202897B1 (en) 1979-01-19 1979-01-19 1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof

Publications (1)

Publication Number Publication Date
CS202897B1 true CS202897B1 (en) 1981-02-27

Family

ID=5336381

Family Applications (1)

Application Number Title Priority Date Filing Date
CS43379A CS202897B1 (en) 1979-01-19 1979-01-19 1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof

Country Status (1)

Country Link
CS (1) CS202897B1 (cs)

Similar Documents

Publication Publication Date Title
IE60157B1 (en) 2-Hydroxy-3-phenoxypropyl amines
JPS61210091A (ja) 新規なジホスホネ−ト
US4032644A (en) Isoxazolyl benzoic acids
GB1351095A (en) N-caboxylated n-methylcarbamic acid aryl esters process for their production and their insecticidal and acaricidal use
CS202897B1 (en) 1-phenyl-2-/4/2-hydroxyethoxy/phenyl/-1,2-ethandione and process for preparing thereof
JPH0419999B2 (cs)
SU467517A3 (ru) Способ получени аминопроизводных бензофенона
US5012000A (en) Total synthesis of chiral 2-amino-1,3-diols
US4933449A (en) Preparing 3-(4 chlorophenyl)-3-(3,4-dimethoxyphenyl) acrylic acid morpholide in the presence of potassium tert-butylate
SU1041545A1 (ru) Конденсированные производные @ -триазина,про вл ющие антидепрессивную активность
JPS58128340A (ja) フェニルエチレン誘導体及びその製法
SU510993A3 (ru) Способ получени перфторалкиламиноалканолов
JPS57175164A (en) 1,4-dihydropyridine derivative and its preparation
RU2342369C1 (ru) Способ получения 5-[4-(1,3,5-дитиазинан-5-сульфонил)-фенил]-1,3,5-дитиазинана
JPH0437812B2 (cs)
Yahyaei et al. Experimental and theoretical studies of diethyl 2-(ter-butylimino)-2, 5-dihydro-5-oxo-1-phenyl-1H-pyrrole-3, 4-dicarboxylate using DFT calculations
JPH0247992B2 (ja) Benzofuenonn22karubameetojudotai
Foye et al. Dithiobiuret analogs of tibione
SU689620A3 (ru) Способ получени бензо-2,4-тиазепинов
EP0005186B1 (de) 3-Alkyl-5-(2-hydroxy-styryl)-isoxazole und Verfahren zu ihrer Herstellung
SU1735263A1 (ru) Способ получени 1-фенил-1-хлор-3-метоксипропана
SU551334A1 (ru) Способ получени изотиуронийдиметилфосфатов
SU1198056A1 (ru) Способ получени диалкилацеталей @ -кетоальдегидов
JPS5835505B2 (ja) N−(α−メチル−ベンジル)−脂肪酸アミド
GB1436519A (en) N-sulphenylated n-methyl-carbamates process for their preparation and their use as insecticides or acaricides