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Benzaldehyde → HCID 21825613、化合物

HRID 1818912
ノート
印刷プレビュー

反応式

HRID 1818912 の反応式
[CH3:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[CH:4][CH:3]=1.[Li+].C[Si]([N-][Si](C)(C)C)(C)C.[CH:20](=[O:27])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[Cl-].[NH4+]>O.C1COCC1>[OH:27][CH:20]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[CH:4][CH:3]=1
参加物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 240BenzaldehydeHCID 25517Ammonium ChlorideHCID 2278064-Methyl-3-cyanopyridineHCID 2733832Lithium hexamethyldisilazane

生成物 1

HCID 21825613HCID 21825613、化合物収率 91.1%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

4-methyl-nicotinonitrile (2.0 g, 16.93 mmol) was dissolved in20 mL of anhydrous THF(20 mL), added with LHMDS (1M solution in THF, 34 mL, 33.86 mmol) at −78° C. under the nitrogen atmosphere and then stirred for about 1 hour at the same temperature. The mixture was dropwisely added with benzaldehyde (2.1 mL, 20.32 mmol) and stirred at −50° C. for about 1 hour. The mixture, while being stirred at 0° C., added with 30 mL of saturated solution of ammonium chloride and 50 ML of distilled water, and then extracted twice with 100 ML of EtOAc. The resulting organic layer was washed with a saturated solution of sodium chloride, dried with anhydrous sodium sulfate, filtered and concentrated. A silica gel column chromatography (2% MeOH/MC) was performed on the resulting residue and obtained 3.46 g (91%) of 4-(2-hydroxy-2-phenyl-ethyl)-nicotinonitrile in pale yellow solid.

後処理

  1. stirringstirred at −50° C. for about 1 hour
  2. stirringThe mixture, while being stirred at 0° C.
  3. extractionextracted twice with 100 ML of EtOAc
  4. washThe resulting organic layer was washed with a saturated solution of sodium chloride
  5. dry with materialdried with anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-b20619d637bf4c9f8a0319fa85a3eed3
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07601736B2

反応ノート

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