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Trifluoroacetic acid → 4-Cyano-2-isobutylpyridine

HRID 660032
ノート
印刷プレビュー

反応式

HRID 660032 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1)#[N:2].C(O)(=O)[CH2:10][CH:11]([CH3:13])[CH3:12].FC(F)(F)C(O)=O.[OH-].[Na+]>[N+]([O-])([O-])=O.[Ag+].ClC1C=CC=CC=1.O>[C:1]([C:3]1[CH:8]=[CH:7][N:6]=[C:5]([CH2:10][CH:11]([CH3:13])[CH3:12])[CH:4]=1)#[N:2]
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

7

反応物 4

HCID 6422Trifluoroacetic acidHCID 75064-CyanopyridineHCID 10430Isovaleric AcidHCID 14798Sodium Hydroxide

生成物 1

HCID 146417864-Cyano-2-isobutylpyridine収率 54%

試薬・触媒・溶媒 2

HCID 24470Silver Nitrate触媒
HCID 19815812
Chlorobenzene water
溶媒

反応条件

温度
0 °C

実験手順

p-cyanopyridine (8.00 g, 76.8 mmol) was added to a 1:1 mixture of chlorobenzene/water (1.5 L) in a 2 L round-bottom flask. Isovaleric acid (21.74 g, 212.8 mmol), (NH4)2S2O8 (34.40 g, 150.7 mmol), trifluoroacetic acid (8.78 g, 77.0 mmol) and AgNO3 (1.040 g, 6.1 mmol) were added and the heterogeneous mixture was vigorously stirred and refluxed for 2 h. The reaction was cooled down to 0° C. and 8 M NaOH was added slowly until pH 9-10. The mixture was filtered through Celite and extracted with EtOAc (×3). The combined organic extracts were dried with MgSO4 and the solvent removed in vacuo. The dark-brown oil was purified via flash chromatography (1:4 EtOAc/Hexane) to give a brown oil (6.538 g, 54%);

後処理

  1. temperaturerefluxed for 2 h
  2. filtrationThe mixture was filtered through Celite
  3. extractionextracted with EtOAc (×3)
  4. dry with materialThe combined organic extracts were dried with MgSO4
  5. customthe solvent removed in vacuo
  6. customThe dark-brown oil was purified via flash chromatography (1:4 EtOAc/Hexane)

出典と根拠

ORDレコード
ord-1bc1b13d81f64304970f530af7fa27c3
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08084471B2

反応ノート

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