StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Nitromethane → tert-Butyl [1-(2-chlorophenyl)-2-nitroethyl]carbamate

HRID 2402795
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2402795
[N+:1]([CH3:4])([O-:3])=[O:2].C(N(CC)C(C)C)(C)C.[Cl:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1/[CH:21]=[N:22]/[C:23](=[O:29])[O:24][C:25]([CH3:28])([CH3:27])[CH3:26]>>[Cl:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH:21]([NH:22][C:23](=[O:29])[O:24][C:25]([CH3:27])([CH3:26])[CH3:28])[CH2:4][N+:1]([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 6375NitromethaneHCID 81531DiisopropylethylamineHCID 12195069tert-butyl (NE)-N-[(2-chlorophenyl)methylidene]carbamate

Produkt 1

HCID 59536890tert-Butyl [1-(2-chlorophenyl)-2-nitroethyl]carbamate

Versuchsvorschrift

A quantity of 16 ml (295.41 mmol) of nitromethane was admixed with 436 μl (2.50 mmol) of N,N-diisopropylethylamine and the yellow solution was stirred at RT for 1 h. Then 2.0 g (8.34 mmol) of the compound from Example 111A were added and the mixture was stirred overnight at RT. All of the volatile constituents were removed on a rotary evaporator. The residue was dissolved in 9 ml of isopropanol in the heat of boiling, and the solution was then cooled to 0° C. The white solid precipitated was filtered off with suction and washed with a little cold isopropanol. Drying in an HV gave 1.18 g (47% of theory) of the title compound.

Aufarbeitung

  1. stirringthe mixture was stirred overnight at RT
  2. customAll of the volatile constituents were removed on a rotary evaporator
  3. dissolutionThe residue was dissolved in 9 ml of isopropanol in the
  4. temperatureheat
  5. temperaturethe solution was then cooled to 0° C
  6. customThe white solid precipitated
  7. filtrationwas filtered off with suction
  8. washwashed with a little cold isopropanol
  9. customDrying in an HV

Quellen und Nachweise

ORD-Eintrag
ord-a5a26bff30d543a683fbc4ce08101a85
Quelldatensatz
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08796324B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion