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Ammonium Chloride → 6-Tert-butyl-2-methoxynicotinonitrile

HRID 1961486
ノート
印刷プレビュー

反応式

HRID 1961486 の反応式
[C:1]([C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[C:7](Cl)[N:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:14][O-:15].[Na+].[NH4+].[Cl-]>CO>[C:1]([C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[C:7]([O:15][CH3:14])[N:6]=1)([CH3:4])([CH3:3])[CH3:2]
参加物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 25517Ammonium ChlorideHCID 10942334Sodium MethoxideHCID 532788766-Tert-butyl-2-chloropyridine-3-carbonitrile

生成物 1

HCID 667452296-Tert-butyl-2-methoxynicotinonitrile収率 85%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

In a screw cap pressure tube, 6-tert-butyl-2-chloronicotinonitrile (410.0 mg, 2.1 mmol) was dissolved in anhydrous MeOH (3.0 ml) under N2. NaOMe (159.3 mg, 2.9 mmol) was added as a solution in anhydrous MeOH (3.0 ml). The tube was sealed and the mixture refluxed for 20 hours. The mixture was allowed to cool. NH4Cl (sat.) was added and the product extracted with EtOAc. The combined organic extracts were washed with water, dried (MgSO4), filtered and concentrated. Purification was done by flash chromatography (Pet. Ether/EtOAc 95:5) to give the title substance in 85% yield.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customIn a screw cap pressure tube
  2. customThe tube was sealed
  3. temperaturethe mixture refluxed for 20 hours
  4. temperatureto cool
  5. extractionthe product extracted with EtOAc
  6. washThe combined organic extracts were washed with water
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customPurification
  11. customto give the title substance in 85% yield

出典と根拠

ORDレコード
ord-f7b2f1a063814ccdb56407e82ee6d084
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08415333B2

反応ノート

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