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Hydrogen Peroxide → 4-Ethyl-2,4-dihydro-5-(trifluoromethyl)-3H-1,2,4-triazol-3-one

HRID 2294625
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HRID 2294625 반응식
[CH2:1]([N:3]1[C:7]([C:8]([F:11])([F:10])[F:9])=[N:6][NH:5][C:4]1=S)[CH3:2].[OH:13]O>[OH-].[Na+]>[CH2:1]([N:3]1[C:7]([C:8]([F:11])([F:10])[F:9])=[N:6][NH:5][C:4]1=[O:13])[CH3:2]
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참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 157901204-Ethyl-2,4-dihydro-5-(trifluoromethyl)-3H-1,2,4-triazole-3-thione

생성물 1

HCID 110844944-Ethyl-2,4-dihydro-5-(trifluoromethyl)-3H-1,2,4-triazol-3-one수율 58%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

9.9 g (0.05 mol) of 4-ethyl-5-trifluoromethyl-2,4-dihydro-3H-1,2,4-triazole-3-thione and 50 ml of 2.5-molar sodium hydroxide solution are introduced. 17 ml (0.165 mol) of 30% strength hydrogen peroxide solution are added dropwise in the course of 20 minutes at a maximum temperature of 40° C. to 50° C. (cooling), stirring is continued for 6 hours at 40° C., the excess of hydrogen peroxide is removed by adding sodium hydrogen sulphite, and the mixture is acidified using concentrated hydrochloric acid and refluxed for 10 hours. When cold, the mixture is poured into ice-water, this is extracted repeatedly using dichloromethane, the combined organic phases are dried over sodium sulphate, and the solvent is evaporated on a rotary evaporator. 5.2 g (58% of theory) of 4-ethyl-5-trifluoromethyl-2,4-dihydro-3H-1,2,4-triazol-3-one of melting point 53° C. are obtained.

후처리

  1. customthe excess of hydrogen peroxide is removed
  2. additionby adding sodium hydrogen sulphite
  3. temperaturerefluxed for 10 hours
  4. additionWhen cold, the mixture is poured into ice-water
  5. extractionthis is extracted repeatedly using dichloromethane
  6. dry with materialthe combined organic phases are dried over sodium sulphate
  7. customthe solvent is evaporated on a rotary evaporator

출처 및 근거

ORD 기록
ord-53129a29a5b344d4beb84765feaa4f1b
출처 데이터셋
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05688963

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