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Hydrazine → 5-Benzylthiophene-2-carboxylic acid

HRID 894236
ノート
印刷プレビュー

反応式

HRID 894236 の反応式
[C:1]([C:9]1[S:13][C:12]([C:14]([OH:16])=[O:15])=[CH:11][CH:10]=1)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+].NN>C(O)CO>[CH2:1]([C:9]1[S:13][C:12]([C:14]([OH:16])=[O:15])=[CH:11][CH:10]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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

5

反応物 3

HCID 9321HydrazineHCID 14797Potassium HydroxideHCID 1082345879505-01-4

生成物 1

HCID 126787025-Benzylthiophene-2-carboxylic acid

試薬・触媒・溶媒 1

HCID 174Ethylene Glycol溶媒2 回

反応条件

温度
140 °C

実験手順

5-Benzoylthiophene-2-carboxylic acid (1.2 g.) was combined with potassium hydroxide (4 g.), hydrazine (3 ml.) and ethylene glycol (8 ml.) and heated in a 140° C. oil bath. A thick, foamy slurry formed which was diluted with 10 ml. additional ethylene glycol. The bath temperature was increased to 180° C., and the reaction held at this temperature for 45 minutes. The reaction was cooled, filtered and the filtrate diluted with 75 ml. of water. The mixture was cooled in an ice bath, acidified with conc. hydrochloric acid, and product (658 mg.) recovered by filtration. Recrystallization from methanol/water gave purified 5-benzylthiophene-2-carboxylic acid (480 mg., 123°-125° C., m/e 218).

後処理

  1. customA thick, foamy slurry formed which
  2. additionwas diluted with 10 ml
  3. temperatureThe bath temperature was increased to 180° C.
  4. temperatureThe reaction was cooled
  5. filtrationfiltered
  6. additionthe filtrate diluted with 75 ml
  7. temperatureThe mixture was cooled in an ice bath
  8. filtrationrecovered by filtration
  9. customRecrystallization from methanol/water
  10. customgave
  11. custompurified 5-benzylthiophene-2-carboxylic acid (480 mg., 123°-125° C., m/e 218)

出典と根拠

ORDレコード
ord-42e915b416904b529da9a283f6c9b8f9
出典データセット
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04282246

反応ノート

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