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Acetyl chloride → 5-Formylaminomethyl-3-methylisoxazole

HRID 1196858
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1196858
[N+:1]([CH2:4][CH3:5])([O-:3])=O.C[O-].[Na+].[Na].C(Cl)(=O)C.[CH:14]([NH:16][CH2:17][C:18]#[CH:19])=[O:15]>CN(C)C(=O)C.CO>[CH:14]([NH:16][CH2:17][C:18]1[O:3][N:1]=[C:4]([CH3:5])[CH:19]=1)=[O:15]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 6367Acetyl chlorideHCID 6587NitroethaneHCID 5360545SodiumHCID 9855445N-(prop-2-yn-1-yl)formamideHCID 10942334Sodium Methoxide

Produkt 1

HCID 179326965-Formylaminomethyl-3-methylisoxazole

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887
Methanol
Lösungsmittel
HCID 31374DimethylacetamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

A stirred solution of nitroethane (17.9 ml, 0.25 mol) in N,N-dimethylacetamide (DMA) (250 ml) was added dropwise at 25°-30° C. to a solution of sodium methoxide, prepared by dissolving sodium (5.75 g) in dry methanol. The reaction mixture was cooled to 5° C. and acetyl chloride (18.5 ml, 0.26 mol) was added at 5°-10° C. Then was added a solution of 3-formylaminopropyn (17 g, 0.20 mol) in DMA (15 ml), and stirring was continued at room temperature overnight. The solvent was removed in vacuo and the residue was extracted with ether (300 ml). The ether was evaporated leaving an oily residue from which the title compound was isolated by distillation (120°-140° C./0.3 mmHg); 1H-NMR (CDCl3) 2.21 (s,3H), 4.35 (d,2H), 5.97 (s,1H), 7-8 (br, 1H), 8.13 (s,1H). (Compound 15).

Aufarbeitung

  1. customprepared
  2. customThe solvent was removed in vacuo
  3. extractionthe residue was extracted with ether (300 ml)
  4. customThe ether was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-696d3c6fac014446b44ee9b72b32d537
Quelldatensatz
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05116841

Notizen zur Reaktion

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