Carbon Dioxide → 4-Cyano-3-methylbenzoic acid

HRID 227224ノート

反応式

HRID 227224 の反応式
Br[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([CH3:10])[CH:3]=1.C([Li])CCC.[C:16](=[O:18])=[O:17].O>C1COCC1>[C:6]([C:5]1[CH:8]=[CH:9][C:2]([C:16]([OH:18])=[O:17])=[CH:3][C:4]=1[CH3:10])#[N:7]

参加物

6

反応物 4

HCID 280Carbon DioxideHCID 962WaterHCID 1442674-Bromo-2-methylbenzonitrileHCID 178418339Butyllithium

生成物 1

HCID 102410994-Cyano-3-methylbenzoic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

To a solution of 4-bromo-2-methylbenzonitrile (2.0 g, 10.2 mmol) in THF (100 ml) at −78° C. under a nitrogen atmosphere was added dropwise a 2.5M solution of n-butyl lithium (4.48 ml, 11.2 mmol). The mixture was stirred at −78° C. for 1 h and then poured onto solid carbon dioxide (5 g) in THF (50 ml). The mixture was allowed to warm to room temperature. Water was added (200 ml) and the mixture was extracted with diethyl ether (3 times). The aqueous layer was acidified by addition of concentrated HCl and extracted with chloroform (3 times). The combined chloroform extracts were washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid; yield 1.2 g (73%).

後処理

  1. temperatureto warm to room temperature
  2. extractionthe mixture was extracted with diethyl ether (3 times)
  3. additionThe aqueous layer was acidified by addition of concentrated HCl
  4. extractionextracted with chloroform (3 times)
  5. washThe combined chloroform extracts were washed with water
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customto give a white solid

出典と根拠

ORDレコード
ord-b69d8e0acdec453e822fb8ec30006b53
出典データセット
uspto-grants-2009_07
特許番号
US07560454B2

反応ノート

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