Phosgene → HCID 23042069、化合物
反応式
[Cl: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)=[O:24].C(N(CC)CC)C>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[C:3]=1[C:4]1[O:5][C:23](=[O: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]=1参加物
実験手順
2.5 g (7.5 mmol) of 2-chloro-6-fluoro-N'-(α,α,α-trifluoro-o-tolyl)-benzhydrazide are heated to reflux temperature (internal temperature 80° C.) for 16 hours in 35 ml of a 20% solution of phosgene (67 mmol) in toluene. Excess phosgene and toluene are then distilled off, and the residue is dissolved in 30 ml of methylene chloride and heated to reflux temperature for 30 minutes with the addition of 6.7 ml (48 mmol) of triethylamine. The mixture is subsequently washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. After chromatographic purification of the crude product with toluene/n-hexane (1:1) as the eluent and recrystallization from methylene chloride/n-hexane there is obtained pure 5-(2-chloro-6-fluorophenyl)-3-(α,α,α-trifluoro-o-tolyl)-1,3,4-oxadiazol-2(3H)-one, m.p. 109°-109.5° C.; IR spectrum: 1792 cm-1 ; mass spectrum: 358(14), 314(23), 159(100).
後処理
- distillationExcess phosgene and toluene are then distilled off
- dissolutionthe residue is dissolved in 30 ml of methylene chloride
- temperatureheated
- temperatureto reflux temperature for 30 minutes
- washThe mixture is subsequently washed with water
- dry with materialdried over anhydrous sodium sulfate
- customevaporated under reduced pressure
- customAfter chromatographic purification of the crude product with toluene/n-hexane (1:1)
- customas the eluent and recrystallization from methylene chloride/n-hexane there
出典と根拠
- ORDレコード
- ord-9fcac8b1f83a4f22acd9c680dd5d7a13
- 出典データセット
- uspto-grants-1990_07
- 特許番号
- US04943583
反応ノート
読み込み中…