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Propionic anhydride → CID 367964

HRID 47632
ノート
印刷プレビュー

反応式

HRID 47632 の反応式
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[C:10]([O:14]C(=O)CC)(=[O:13])[CH2:11][CH3:12].C([O-])(=O)CC.[Na+]>>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[C:11]([CH3:12])[C:10]([OH:14])=[O:13])=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 31263Propionic anhydrideHCID 680234-FluorobenzaldehydeHCID 2723816Sodium Propionate

生成物 1

HCID 367964CID 367964

反応条件

温度
140 °C

実験手順

p-Fluorobenzaldehyde (200 g, 1.61 mol), propionic anhydride (3.5 g, 2.42 mol) and sodium propionate (155 g, 1.61 mol) are mixed in a one liter three-necked flask which had been flushed with nitrogen. The flask is heated gradually in an oil-bath to 140° C. After 20 hours, the flask is cooled to 100° C. and poured into 8 l of water. The precipitate is dissolved by adding potassium hydroxide (302 g) in 2 l of water. The aqueous solution is extracted with ether, and the ether extracts are washed with potassium hydroxide solution. The combined aqueous layers are filtered, are acidified with concentrated HCl, and are filtered. The collected solid, p-fluoro-α-methylcinnamic acid, is washed with water, and is dried and used as obtained.

後処理

  1. customhad been flushed with nitrogen
  2. temperaturethe flask is cooled to 100° C.
  3. additionpoured into 8 l of water
  4. dissolutionThe precipitate is dissolved
  5. additionby adding potassium hydroxide (302 g) in 2 l of water
  6. extractionThe aqueous solution is extracted with ether
  7. washthe ether extracts are washed with potassium hydroxide solution
  8. filtrationThe combined aqueous layers are filtered
  9. filtrationare filtered
  10. washThe collected solid, p-fluoro-α-methylcinnamic acid, is washed with water
  11. customis dried
  12. customas obtained

出典と根拠

ORDレコード
ord-6efc3b3c28c54bd1a91d9c35dff01a04
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06699894B1

反応ノート

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