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Triethylamine → HCID 23042139, 화합물

HRID 2166089
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HRID 2166089 반응식
[F:1][C:2]1[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[C:3]=1[C:4]([NH:6][NH:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[C:14]([F:17])([F:16])[F:15])=[O:5].[C:23](Cl)(Cl)=[S:24].C(N(CC)CC)C>C1(C)C=CC=CC=1.COC(C)(C)C>[F:1][C:2]1[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[C:3]=1[C:4]1[O:5][C:23](=[S:24])[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]([F:15])([F:16])[F:17])[N:6]=1
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참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 10040ThiophosgeneHCID 23042045HCID 23042045, 화합물

생성물 1

HCID 23042139HCID 23042139, 화합물

시약·촉매·용매 2

HCID 1140Toluene용매HCID 15413tert-Butyl methyl ether용매

실험 절차

4.79 g (15 mmol) of 2,6-difluoro-N'-(α,α,α-trifluoro-o-tolyl)-benzhydrazide in 30 ml of toluene are treated with 1.98 g (17 mmol) of thiophosgene and the reaction mixture is heated at the reflux temperature for 5 hours. 4.8 ml (35 mmol) of triethylamine are then added dropwise at 45° C. while cooling and, after cooling, the mixture is stirred at room temperature for about 1 hour. The mixture is subsequently taken up in 100 ml of tert.butyl methyl ether and the solution is washed in each case once with dilute, ice-cold sodium hydroxide solution and saturated sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue is purified by chromatography using acetone/n-hexane (1:4) as the eluent and crystallized from diisopropyl ether/n-hexane. In this manner there is obtained 5-(2,6-difluorophenyl)-3-(α,α,α-trifluoro-o-tolyl)-1,3,4-oxadiazole-2(3H) -thione as a white crystallizate, m.p. 128°-130° C.; mass spectrum: 358(58), 298(15 ), 289(17), 159(100).

후처리

  1. temperaturethe reaction mixture is heated at the reflux temperature for 5 hours
  2. temperaturewhile cooling
  3. temperatureafter cooling
  4. washthe solution is washed in each case once
  5. additionwith dilute
  6. dry with materialice-cold sodium hydroxide solution and saturated sodium chloride solution, dried over anhydrous magnesium sulfate
  7. customevaporated under reduced pressure
  8. customThe residue is purified by chromatography
  9. customcrystallized from diisopropyl ether/n-hexane

출처 및 근거

ORD 기록
ord-31cf73efbc9b405bae325600f57d2e29
출처 데이터셋
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04943583

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