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Water → 7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-one

HRID 569691
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 569691
[F:1][C:2]1[CH:3]=[CH:4][C:5]([N+:15]([O-])=O)=[C:6]([CH:14]=1)[O:7][CH2:8][C:9](OCC)=[O:10].O>C(O)(=O)C.[Fe]>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:15][C:9](=[O:10])[CH2:8][O:7][C:6]=2[CH:14]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 962WaterHCID 13752803Ethyl 2-(5-fluoro-2-nitrophenoxy)acetate

Produkt 1

HCID 137312957-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneAusbeute 74,8 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23925IronKatalysatorHCID 176Acetic AcidLösungsmittel2×

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A solution of the 49.0 grams (0.20 mole) of ethyl 2-(5-fluoro-2-nitrophenoxy)acetate in 100 ml of glacial acetic acid was added to a warm (60° C.), stirred mixture of iron powder (50.0 grams, 0.90 mole) in 300 ml of glacial acetic acid. The reaction temperature was allowed to reach 100° C., and the mixture was stirred for approximately three hours. This mixture was poured into water, forming a precipitate. The precipitate was collected by filtration and was recrystallized from ethanol to yield 25.0 grams of 7-fluoro-2H-1,4-benzoxazin-3(4H)-one; another sample of this compound prepared in a similar manner, and then purified further, had a melting point of 205°-206° C. and an nmr spectrum which was consistent with the proposed structure.

Aufarbeitung

  1. customto reach 100° C.
  2. stirringthe mixture was stirred for approximately three hours
  3. customforming a precipitate
  4. filtrationThe precipitate was collected by filtration
  5. customwas recrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-d498f89c67c34a9ca9cbc1c1fb0756a8
Quelldatensatz
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04734124

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