Benzyl Alcohol → 3-(Benzyloxy)pyridine-4-carbonitrile

HRID 1913755ノート

反応式

HRID 1913755 の反応式
[H-].[Na+].[CH2:3]([OH:10])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl[C:12]1[CH:19]=[N:18][CH:17]=[CH:16][C:13]=1[C:14]#[N:15]>CN(C=O)C>[CH2:3]([O:10][C:12]1[CH:19]=[N:18][CH:17]=[CH:16][C:13]=1[C:14]#[N:15])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1

参加物

5

反応物 3

HCID 244Benzyl AlcoholHCID 24758Sodium hydrideHCID 106783063-Chloropyridine-4-carbonitrile

生成物 1

HCID 108223413-(Benzyloxy)pyridine-4-carbonitrile収率 87%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 0.59 g of 60% sodium hydride (in oil) and 5 ml of DMF was stirred while ice-cooling. To the reaction mixture, 1.59 g of benzyl alcohol was added. The reaction mixture was stirred at the same temperature for 10 minutes. To the reaction mixture, 2.0 g of 3-chloroisonicotinonitrile was added, and the reaction mixture was stirred at the same temperature for 30 minutes and at room temperature for 1.5 hours. The reaction mixture was concentrated under reduced pressure, and then to ethyl acetate was added to the reaction mixture, followed by filtration of insoluble matters. The filtrate was concentrated under reduced pressure and the resultant residue was subjected to silica gel column chromatography to give 2.64 g of 3-benzyloxy isonicotinonitrile.

後処理

  1. temperaturecooling
  2. stirringThe reaction mixture was stirred at the same temperature for 10 minutes
  3. stirringthe reaction mixture was stirred at the same temperature for 30 minutes and at room temperature for 1.5 hours
  4. concentrationThe reaction mixture was concentrated under reduced pressure
  5. additionto ethyl acetate was added to the reaction mixture
  6. filtrationfollowed by filtration of insoluble matters
  7. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-70f7effa65094ba6b4afd49b1700766e
出典データセット
uspto-grants-2013_12
特許番号
US08609705B2

反応ノート

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