Phosphorus pentachloride → 3-Chlorothiophene-2-carboxylic acid

HRID 27999

反応式

HRID 27999 の反応式
P(Cl)(Cl)(Cl)(Cl)[Cl:2].O[C:8]1[CH:12]=[CH:11][S:10][C:9]=1[C:13]([O:15]C)=[O:14]>C(Cl)(Cl)(Cl)Cl>[Cl:2][C:8]1[CH:12]=[CH:11][S:10][C:9]=1[C:13]([OH:15])=[O:14]

参加物

4

反応物 2

HCID 24819Phosphorus pentachlorideHCID 5811273-Hydroxy-thiophene-2-carboxylic acid methyl ester

生成物 1

HCID 7012693-Chlorothiophene-2-carboxylic acid

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒2 回

実験手順

52.1 g. of phosphorus pentachloride are dissolved in 600 ml. of absolute carbon tetrachloride and heated to boiling, whereupon a solution of 15.8 g. of 3-hydroxy-2-methoxycarbonyl-thiophene in 200 ml. of carbon tetrachloride is added dropwise during 3 hours. The mixture is boiled to reflux for 13 hours, the carbon tetrachloride is distilled off and the mixture is evaporated almost to dryness in vacuo. 450 Ml. of water are added dropwise while cooling, whereupon the mixture is heated to boiling and then allowed to cool. The resulting precipitate is filtered off under suction and boiled up with 10 g. of active carbon in a solution of 25 g. of sodium bicarbonate. The active carbon is then filtered off under suction and the cooled solution is acidified with hydrochloric acid. There is obtained 3-chlorothiophene-2-carboxylic acid of melting point 185°-186° C.

後処理

  1. temperatureto reflux for 13 hours
  2. distillationthe carbon tetrachloride is distilled off
  3. customthe mixture is evaporated almost to dryness in vacuo
  4. additionof water are added dropwise
  5. temperaturewhile cooling, whereupon the mixture
  6. temperatureis heated
  7. temperatureto cool
  8. filtrationThe resulting precipitate is filtered off under suction
  9. filtrationThe active carbon is then filtered off under suction

出典と根拠

ORDレコード
ord-f7b094aa829e4778819c92be1a50b47e
出典データセット
uspto-grants-1980_09
特許番号
US04224445

関連ノート

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