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Water → Benzoic acid, 4-(acetylamino)-2-hydroxy-3-(2-propenyl)-, methyl ester

HRID 1084943
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1084943
C([O:4][C:5]1[CH:14]=[C:13]([NH:15][C:16]([CH3:18])=[O:17])[CH:12]=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8])C=C.O.CN1C[CH2:24][CH2:23][C:22]1=O>>[OH:4][C:5]1[C:14]([CH2:24][CH:23]=[CH2:22])=[C:13]([NH:15][C:16]([CH3:18])=[O:17])[CH:12]=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 962WaterHCID 13387N-methyl-2-pyrrolidone2×HCID 10586690HCID 10586690, Verbindung2×

Produkt 1

HCID 10800613Benzoic acid, 4-(acetylamino)-2-hydroxy-3-(2-propenyl)-, methyl ester

Versuchsvorschrift

84 g of methyl 2-allyloxy-4-acetaminobenzoate and 84 g of N-methylpyrrolidone were introduced into a 500 ml round-bottomed flask. The contents were heated quickly to reflux which was then maintained for 30 minutes, and the solution was then cooled slightly and poured into water. Crystallation was immediate. The same operations were repeated with the same quantities of methyl 2-allyloxy-4-acetaminobenzoate and N-methylpyrrolidone and the products from the two trials were combined and cooled, drained, washed with water and dried at 50° C.

Aufarbeitung

  1. temperatureThe contents were heated quickly
  2. temperatureto reflux which
  3. temperaturewas then maintained for 30 minutes
  4. temperaturethe solution was then cooled slightly
  5. temperaturecooled
  6. washwashed with water
  7. customdried at 50° C.

Quellen und Nachweise

ORD-Eintrag
ord-e8b5768364bb496f8a1b6f690452ecad
Quelldatensatz
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05006570

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