Carbon Dioxide → 4-(Dimethylamino)but-2-ynoic acid

HRID 379148ノート

反応式

HRID 379148 の反応式
C([Li])CCC.[CH3:6][N:7]([CH3:11])[CH2:8][C:9]#[CH:10].[C:12](=[O:14])=[O:13].O>CCCCCC.O1CCCC1.CO>[CH3:6][N:7]([CH3:11])[CH2:8][C:9]#[C:10][C:12]([OH:14])=[O:13]

参加物

8

反応物 4

HCID 280Carbon DioxideHCID 962WaterHCID 81643N,N-DimethylpropargylamineHCID 178418339Butyllithium

生成物 1

HCID 150797524-(Dimethylamino)but-2-ynoic acid

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒HCID 8058Hexane溶媒

反応条件

温度
-78 °C

実験手順

n-Butyl lithium in hexane (96 mL, 2.5 M in n-hexane) was slowly added to 1-dimethylamino-2-propyne (20 g, 240 mmol) in 100 mL of tetrahydrofuran under nitrogen. The mixture was stirred for 1 h at −78° C., then dry carbon dioxide was pass through overnight. The resulting solution was poured into water and washed with ethyl acetate. The aqueous layer was evaporated under reduced pressure to give the crude acid. The dry acid was dissolved in methanol, and the insoluble salt was removed via filtration. The filtrate was collected and dried in vacuo to give 15.6 g of 4-dimethylamino-but-2-ynoic acid: mass spectrum (m/e): M−H 126.

後処理

  1. customthrough overnight
  2. washwashed with ethyl acetate
  3. customThe aqueous layer was evaporated under reduced pressure
  4. customto give the crude acid
  5. customthe insoluble salt was removed via filtration
  6. customThe filtrate was collected
  7. customdried in vacuo

出典と根拠

ORDレコード
ord-33d35dca479141c7b0f23a4c828c0d0d
出典データセット
uspto-grants-2001_10
特許番号
US06297258B1

反応ノート

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