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Hydrochloric Acid → 8-Chloro-5-methoxy-2-methylquinoline hydrochloride

HRID 1051549
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1051549
[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([O:9][CH3:10])=[CH:5][C:3]=1[NH2:4].Cl.[C:12]1(Cl)[C:18](=O)C(Cl)=C(Cl)[C:14](=O)[C:13]=1Cl.C(=O)/C=C/C>C(O)CCC.O1CCCC1>[ClH:1].[Cl:1][C:2]1[CH:8]=[CH:7][C:6]([O:9][CH3:10])=[C:5]2[C:3]=1[N:4]=[C:13]([CH3:14])[CH:12]=[CH:18]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 8371ChloranilHCID 754606-Chloro-m-anisidineHCID 447466Crotonaldehyde

Produkt 1

HCID 754807178-Chloro-5-methoxy-2-methylquinoline hydrochlorideAusbeute 214,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 263
1-Butanol
Lösungsmittel
2×
HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A 1000-mL 3-necked round-bottom flask was charged with 2-chloro-5-methoxyaniline (50 g, 317 mmol), n-butanol (120 mL), concentrated hydrochloric acid (37%, 90 mL), and chloranil (tetrachloro-1,4-benzoquinone) (78 g, 317 mmol). The resulting solution stirred for 1 h at 100° C. in an oil bath. A solution of (E)-crotonaldehyde (28.9 mL, 349 mmol) in n-butanol (50 mL) was added dropwise over 1 h. The resulting solution stirred for 1 h at 100° C. in an oil bath and was then cooled to 70° C. Tetrahydrofuran (650 mL) was added, and the reaction mixture stirred for 1 h at 70° C. and was then cooled to 0° C. The resulting precipitate was held at 0-5° C. for 1 h. The mixture was filtered, the solids were washed with cold (ca. 0° C.) THF (2×350 mL), and then dried in an oven to afford 8-chloro-5-methoxy-2-methylquinoline hydrochloride (83.0 g, 74%) as a yellow solid. MS (ES, m/z): 208 [M+H]+

Aufarbeitung

  1. stirringThe resulting solution stirred for 1 h at 100° C. in an oil bath
  2. temperaturewas then cooled to 70° C
  3. stirringthe reaction mixture stirred for 1 h at 70° C.
  4. temperaturewas then cooled to 0° C
  5. waitThe resulting precipitate was held at 0-5° C. for 1 h
  6. filtrationThe mixture was filtered
  7. washthe solids were washed with cold (ca. 0° C.) THF (2×350 mL)
  8. customdried in an oven

Quellen und Nachweise

ORD-Eintrag
ord-7876ff8af06b4157888e63d67341a69a
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09388161B2

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