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Nitroethane → 2-Hydroxy-4-methoxybenzonitrile

HRID 719120
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 719120
[OH:1][C:2]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[CH:6][C:3]=1[CH:4]=O.C([O-])(=O)C.[Na+].[N+:17](CC)([O-])=O>C(O)(=O)C>[OH:1][C:2]1[CH:9]=[C:8]([O:10][CH3:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6587NitroethaneHCID 696002-Hydroxy-4-MethoxybenzaldehydeHCID 517045Sodium Acetate

Produkt 1

HCID 114236802-Hydroxy-4-methoxybenzonitrileAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

A mixture of the 2-hydroxy-4-methoxybenzaldehyde (20 g, 128.8 mmol), sodium acetate (35.05 g, 257.6 mmol) and nitroethane (19 mL, 257.6 mmol) in glacial acetic acid (100 mL) was heated at gentle reflux for 12 h. The reaction mixture was then poured into ˜1000 mL of ice water (1:1 ratio of ice and water). The product was extracted with ethyl acetate (3×200 mL). The organic extracts were washed with sodium bicarbonate solution until the aqueous layer had pH ˜8. The organic layers were then dried over anhydrous magnesium sulfate and concentrated in vacuo to afford 2-hydroxy-4-methoxy-benzonitrile as a yellow oil (16.5 g, 86%). It was used without further purification.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat gentle reflux for 12 h
  3. extractionThe product was extracted with ethyl acetate (3×200 mL)
  4. washThe organic extracts were washed with sodium bicarbonate solution until the aqueous layer
  5. dry with materialThe organic layers were then dried over anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-e5a769c3bc2d4c87bb9b20d92c92ebdd
Quelldatensatz
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07132421B2

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