Acetic Anhydride → 2-Chloro-3-(2-nitroethenyl)pyridine

HRID 716012

Reaktionsgleichung

Reaktionsgleichung von HRID 716012
Cl[C:2]1[N:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[ClH:10].[CH2:11]([NH2:13])C.[OH-:14].[Na+].C(N(CC)CC)C.C(OC(=O)C)(=[O:25])C.C([O-])(O)=O.[Na+]>[N+](C)([O-])=O.C(O)C.CN(C)C1C=CN=CC=1>[Cl:10][C:2]1[C:3](/[CH:4]=[CH:11]/[N+:13]([O-:25])=[O:14])=[CH:6][CH:7]=[CH:8][N:9]=1

Komponenten

10

Edukt 6

HCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 11198Ethylamine hydrochlorideHCID 14798Sodium HydroxideHCID 516892Sodium BicarbonateHCID 7376072-Chloro-3-pyridinecarboxaldehyde

Produkt 1

HCID 866478022-Chloro-3-(2-nitroethenyl)pyridine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 142844-(Dimethylamino)pyridineKatalysatorHCID 702EthanolLösungsmittelHCID 6375NitromethaneLösungsmittel

Versuchsvorschrift

To 2-chloronicotinaldehyde (2.8 g, 19.8 mmol) in nitromethane (6.1 g) was added ethylamine hydrochloride (100 mg, 1.2 mmol) and NaOH (25 mg) in ethanol (1.5 mL). The mixture was stirred for 1 hour and concentrated. The crude was dissolved in CH2Cl2 (30 mL) and treated with triethylamine (2.8 g, 28 mmol), 4-(dimethylamino)pyridine (20 mg) and acetic anhydride (2.0 g, 20 mmol) at 0° C. The mixture was stirred for 15 minutes and concentrated saturated NaHCO3(aq) was added, and the precipitates were collected to afford the title compound.

Aufarbeitung

  1. concentrationconcentrated
  2. dissolutionThe crude was dissolved in CH2Cl2 (30 mL)
  3. stirringThe mixture was stirred for 15 minutes
  4. customthe precipitates were collected

Quellen und Nachweise

ORD-Eintrag
ord-04009455b9f14af6a61938db44567b12
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09187483B2

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