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4-Hydroxybenzoic acid hydrazide → 4-(5-{[4-Chloro-3-(trifluoromethyl)-phenyl]amino}-1,3,4-oxadiazol-2-yl)phenol

HRID 387458
ノート
印刷プレビュー

反応式

HRID 387458 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([NH:8][NH2:9])=[O:7])=[CH:4][CH:3]=1.[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]=[C:20]=S)=[CH:15][C:14]=1[C:22]([F:25])([F:24])[F:23].CCOC(C)=O.CO>CO.[Hg]=O>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([NH:19][C:20]2[O:7][C:6]([C:5]3[CH:10]=[CH:11][C:2]([OH:1])=[CH:3][CH:4]=3)=[N:8][N:9]=2)=[CH:15][C:14]=1[C:22]([F:23])([F:24])[F:25]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 17424-Hydroxybenzoic acid hydrazideHCID 5200261-Chloro-4-isothiocyanato-2-(trifluoromethyl)benzeneHCID 21584119Ethylacetate methanol

生成物 1

HCID 1361796924-(5-{[4-Chloro-3-(trifluoromethyl)-phenyl]amino}-1,3,4-oxadiazol-2-yl)phenol収率 60.8%

試薬・触媒・溶媒 2

HCID 30856Mercuric oxide触媒
HCID 887
Methanol
溶媒

実験手順

Mercury (II) oxide (yellow) (4.55 g, 21.0 mmol) was suspended in 60 mL of anhydrous MeOH under Ar. A bright-orange suspension was formed. To this suspension was added 4-hydroxybenzoic acid hydrazide (3.20 g, 21.0 mmol) and 4-chloro-3-trifluoromethyl-phenylisothiocyanate (5.0 g, 21.0 mmol). The reaction mixture was refluxed for 2 hours. The solvent was removed in vacuo. The black residue was redissolved in 100 mL of EtOAc and the resulting black suspension was filtered through a short pad of silica gel. The filtrate was mixed with 10 g of dry silica gel and solvent was removed in vacuo. The impregnated silica gel was loaded on silica gel column and the product was separated using a gradient of hexane:ethyl acetate mixture starting from 50:50 ratio and finishing at 0:100. All fractions containing the product were combined; solvent was removed in vacuo to give a grey solid. The solid was heated in 50 mL of 4:1 mixture of EtOAc/MeOH. The formed suspension was cooled down to ambient temperature and filtered to give the title product as a white crystalline solid (4.54 g, 60.7% yield).

後処理

  1. customA bright-orange suspension was formed
  2. temperatureThe reaction mixture was refluxed for 2 hours
  3. customThe solvent was removed in vacuo
  4. dissolutionThe black residue was redissolved in 100 mL of EtOAc
  5. filtrationthe resulting black suspension was filtered through a short pad of silica gel
  6. additionThe filtrate was mixed with 10 g of dry silica gel and solvent
  7. customwas removed in vacuo
  8. customthe product was separated
  9. additionAll fractions containing the product
  10. customsolvent was removed in vacuo
  11. customto give a grey solid
  12. filtrationfiltered

出典と根拠

ORDレコード
ord-47c43d0f85c849f79b881df73daf1190
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08372971B2

反応ノート

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