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Phosphorus pentachloride → 3-Chlorothiophene-2-carboxylic acid

HRID 27999
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반응식

HRID 27999 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

HCID 7012693-Chlorothiophene-2-carboxylic acid

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f7b094aa829e4778819c92be1a50b47e
출처 데이터셋
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04224445

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