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Tetrahydrofuran → 5-[(4-Ethenylphenyl)oxy]-2-(trifluoromethyl)pyrimidine

HRID 474657
ノート
印刷プレビュー

反応式

HRID 474657 の反応式
[H-].[Na+].[F:3][C:4]([F:21])([F:20])[C:5]1[N:10]=[CH:9][C:8]([O:11][C:12]2[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][CH:13]=2)=[CH:7][N:6]=1.[CH2:22]1COCC1>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH:16]([C:15]1[CH:18]=[CH:19][C:12]([O:11][C:8]2[CH:7]=[N:6][C:5]([C:4]([F:21])([F:20])[F:3])=[N:10][CH:9]=2)=[CH:13][CH:14]=1)=[CH2:22]
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

5

反応物 3

HCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 866231314-{[2-(Trifluoromethyl)-5-pyrimidinyl]oxy}benzaldehyde

生成物 1

HCID 677758455-[(4-Ethenylphenyl)oxy]-2-(trifluoromethyl)pyrimidine収率 60.4%

試薬・触媒・溶媒 1

HCID 74505Methyltriphenyliphosphonium bromide触媒

反応条件

温度
0 °C

実験手順

To a suspension of NaH (373 mg, 9.32 mmol) and methyltriphenylphosphonium bromide (799 mg, 2.237 mmol) in THF (5 mL), which was stirred at 0° C. for 1 h was added 4-{[2-(trifluoromethyl)-5-pyrimidinyl]oxy}benzaldehyde (500 mg, 1.864 mmol). The mixture was stirred at room temperature for 2 h, and then quenched with NH4Cl sat. solution. The organic layer was separated and the aqueous phase was extracted with DCM. The organic phase was dried over sodium sulfate, filtered, and concentrated. Purification via flash chromatography then afforded the title compound (300 mg, 1.127 mmol, 60.4% yield).

後処理

  1. stirringThe mixture was stirred at room temperature for 2 h
  2. customquenched with NH4Cl sat. solution
  3. customThe organic layer was separated
  4. extractionthe aqueous phase was extracted with DCM
  5. dry with materialThe organic phase was dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customPurification via flash chromatography

出典と根拠

ORDレコード
ord-d21254a84f1a47ddb7ab5bfff55aa760
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637536B2

反応ノート

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