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Hydrazine → 5-Benzylthiophene-2-carboxylic acid

HRID 894236
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 894236
[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
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 9321HydrazineHCID 14797Potassium HydroxideHCID 1082345879505-01-4

Produkt 1

HCID 126787025-Benzylthiophene-2-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 174Ethylene GlycolLösungsmittel2×

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

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).

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-42e915b416904b529da9a283f6c9b8f9
Quelldatensatz
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04282246

Notizen zur Reaktion

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