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Sodium Hydroxide → 2-Oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acid

HRID 358483
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 358483
[OH-:1].[Na+].BrC(Br)[C:5]([C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH2:11][CH2:10]2)=[O:6]>O>[C:5]([C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH2:11][CH2:10]2)([OH:6])=[O:1]
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Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 131049236-(Dibromoacetyl)-3,4-dihydroquinolin-2(1H)-one

Produkt 1

HCID 71319092-Oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acidAusbeute 54,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Into 250 ml of water, 26 g sodium hydroxide was dissolved, then at a temperature of 90°-100° C. and under stirring condition, 35 g of 6-dibromoacetyl-3,4-dihydrocarbostyril was added thereinto and reacted for 3 hours. After the reaction was completed, the reaction mixture was cooled and insoluble matters formed in the mixture were removed by filtration. The mother liquor was acidified with concentrated hydrochloric acid and the crystals precipitated were collected by filtration and washed with water. The crystals thus obtained were recrystallized from ethanol twice to obtain 10.5 g of 6-carboxy-3,4-dihydrocarbostyril in the form of light yellow amorphous crystals. Melting point: 324.5°-327° C. (decomposed).

Aufarbeitung

  1. additionwas added
  2. customreacted for 3 hours
  3. temperaturethe reaction mixture was cooled
  4. custominsoluble matters formed in the mixture
  5. customwere removed by filtration
  6. customthe crystals precipitated
  7. filtrationwere collected by filtration
  8. washwashed with water
  9. customThe crystals thus obtained
  10. customwere recrystallized from ethanol twice

Quellen und Nachweise

ORD-Eintrag
ord-d71d599c67f74ca480f68de0ffe9a68a
Quelldatensatz
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04468402

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