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Citric Acid → 3-Bromo-1-(4-fluorophenyl)-1h-1,2,4-triazole

HRID 1823998
ノート
印刷プレビュー

反応式

HRID 1823998 の反応式
[Br:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1.[C:7]([OH:10])(=[O:9])[CH3:8].[C:11](O)(=O)[CH3:12].[F:15][C:16]1[CH:21]=[CH:20][C:19]([Bi]([C:30]2[CH:35]=[CH:34][C:33](F)=[CH:32]C=2)C2C=CC(F)=CC=2)=[CH:18][CH:17]=1.[CH3:37]N(C)C(N(C)C)=N.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>O1CCCC1.C([O-])(=O)C.[Cu+2].C([O-])(=O)C.C(OCC)(=O)C.O>[C:7]([O:10][CH2:11][CH3:12])(=[O:9])[CH3:8].[CH3:30][CH2:35][CH2:34][CH:33]([CH3:32])[CH3:37].[F:15][C:16]1[CH:21]=[CH:20][C:19]([N:4]2[CH:5]=[N:6][C:2]([Br:1])=[N:3]2)=[CH:18][CH:17]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

10

反応物 4

HCID 311Citric AcidHCID 664601,1,3,3-TetramethylguanidineHCID 11966511Acetic acid;tris(4-fluorophenyl)bismuthaneHCID 178419478HCID 178419478、化合物

生成物 2

HCID 21882781Isohexane ethyl acetate収率 40%HCID 235711323-Bromo-1-(4-fluorophenyl)-1h-1,2,4-triazole
収率 45%

試薬・触媒・溶媒 4

HCID 8895Cupric acetate触媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
50 °C

実験手順

A mixture of 3-bromo-1,2,4-1H-triazole (prepared as described in Chemische Berichte 1967, 100, 2250) (1.0 g, 6.76 mmol), tri(4-fluorophenyl)bismuth diacetate (prepared by the method described in Synthetic Communications 1996, 4569) (4.53 g, 7.4 mmol), copper (II) acetate (0.25 g, 20 mol %) and N,N,N′,N′-tetramethylguanidine (1.7 mL, 13.5 mmol) in dry tetrahydrofuran (30 mL) was stirred at 50° C. under a balloon of air for 16 hr. The suspension was poured into water (100 mL) and 1M citric acid (30 mL) to give a suspension of pH 3–4. Ethyl acetate (100 mL) was added and the mixture was filtered through Celite®, washing the filter cake with ethyl acetate (100 mL). The two phases of the filtrate were separated and the organic layer was dried (Na2SO4) and concentrated. Flash column chromatography on silica gel, eluting with 25% then 40% ethyl acetate-isohexane, gave 1-(4-fluorophenyl)-3-bromo-1,2,4-1H-triazole as an off-white solid (0.74 g, 45%).

後処理

  1. customprepared by the method
  2. customto give
  3. additiona suspension of pH 3–4
  4. filtrationthe mixture was filtered through Celite®
  5. washwashing the filter cake with ethyl acetate (100 mL)
  6. customThe two phases of the filtrate were separated
  7. dry with materialthe organic layer was dried (Na2SO4)
  8. concentrationconcentrated
  9. washFlash column chromatography on silica gel, eluting with 25%

出典と根拠

ORDレコード
ord-62e2e6d0e7264c9690a9bb60752fe81c
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07041689B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート