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3-Bromoaniline → 5-((3-Bromophenylamino)methylene)-2,2-di-methyl-1,3-dioxane-4,6-dione

HRID 9346
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 9346
[CH:1](OCC)(OCC)OCC.[CH3:11][C:12]1([CH3:20])[O:19][C:17](=[O:18])[CH2:16][C:14](=[O:15])[O:13]1.[Br:21][C:22]1[CH:23]=[C:24]([CH:26]=[CH:27][CH:28]=1)[NH2:25]>C(O)C>[Br:21][C:22]1[CH:23]=[C:24]([NH:25][CH:1]=[C:16]2[C:17](=[O:18])[O:19][C:12]([CH3:20])([CH3:11])[O:13][C:14]2=[O:15])[CH:26]=[CH:27][CH:28]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 115623-Bromoaniline2×HCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 31214Ethyl orthoformate

Produkt 1

HCID 172522195-((3-Bromophenylamino)methylene)-2,2-di-methyl-1,3-dioxane-4,6-dione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Reaktionsbedingungen

Temperatur
55 °C

Versuchsvorschrift

A mixture of triethyl orthoformate (154 grams (g), 1.04 moles (mol) and Meldrum's acid (142 g, 0.983 mol) was heated to 55° C. for 4 hours (h). After cooling to 50° C., a solution of 3-bromoaniline (162.6 g, 0.945 mol) in ethanol (300 mL) was added such that the temperature of the reaction was maintained between 50–55° C. After half of the 3-bromoaniline had been added, stirring became difficult due to the formation of solids, so more ethanol (1 liter (L)) was added to facilitate stirring. Upon complete addition, the reaction was cooled to room temperature (RT), and the solids were collected by filtration. The filter cake was washed with ice cold ethanol until the washings were nearly colorless, and the product was dried at 65° C. under vacuum to afford 287 g of 5-[(3-bromophenylamino)methylene]-2,2-dimethyl-[1,3]dioxane-4,6-dione as an off-white solid.

Aufarbeitung

  1. temperatureAfter cooling to 50° C.
  2. temperaturewas maintained between 50–55° C
  3. additionwas added
  4. stirringto facilitate stirring
  5. additionUpon complete addition
  6. temperaturethe reaction was cooled to room temperature (RT)
  7. filtrationthe solids were collected by filtration
  8. washThe filter cake was washed with ice cold ethanol until the washings
  9. customthe product was dried at 65° C. under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-25de6e20d68e4a01a05d61c43866a6f5
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07091214B2

Notizen zur Reaktion

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