Nitric Acid → 5-Chloro-7-nitro-2,3-dihydro-1-benzofuran

HRID 1654542

Reaktionsgleichung

Reaktionsgleichung von HRID 1654542
S(=O)(=O)(O)O.[Cl:6][C:7]1[CH:8]=[CH:9][C:10]2[O:14][CH2:13][CH2:12][C:11]=2[CH:15]=1.[N+:16]([O-])([OH:18])=[O:17]>O>[Cl:6][C:7]1[CH:8]=[C:9]([N+:16]([O-:18])=[O:17])[C:10]2[O:14][CH2:13][CH2:12][C:11]=2[CH:15]=1

Komponenten

5

Edukt 3

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 5929645-Chloro-2,3-dihydro-1-benzofuran

Produkt 1

HCID 189972445-Chloro-7-nitro-2,3-dihydro-1-benzofuranAusbeute 40,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a stirred and cooled mixture of 32 nil of sulfuric acid and 14 ml of water there were added 17 g of 2,3-dihydro-5-chlorobenzofuran, while keeping the temperature at 25° C. After cooling to 0° C., there were added dropwise 14 ml of nitric acid. Stirring and cooling at 0° C. was continued for 44 hours. The reaction mixture was diluted with water (temp. <10° C.) and stirred for 15 min. The precipitate was filtered off, washed with water and recrystallized from a mixture of ethyl acetate and hexane (30:70), yielding 8.9 g (40.5%) of 5-chloro-2,3-dihydro-7-nitrobenzofuran (interm. 3).

Aufarbeitung

  1. temperaturecooled
  2. customat 25° C
  3. stirringStirring
  4. temperaturecooling at 0° C.
  5. stirringstirred for 15 min
  6. filtrationThe precipitate was filtered off
  7. washwashed with water
  8. customrecrystallized from a mixture of ethyl acetate and hexane (30:70)

Quellen und Nachweise

ORD-Eintrag
ord-94bc4803b7f34d44a1b2d559ff5283ed
Quelldatensatz
uspto-grants-1995_04
Patentnummer
US05407961

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