Benzoic Acid → 5-Nitrocyclohex-1-ene-1-carbaldehyde

HRID 1821122Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1821122
[N+:1]([CH:4]([CH2:9][CH2:10][CH:11]=O)[CH2:5][CH2:6][CH:7]=[O:8])([O-:3])=[O:2].N1CCCC1.C(O)(=O)C1C=CC=CC=1>C(Cl)Cl>[N+:1]([CH:4]1[CH2:5][C:6]([CH:7]=[O:8])=[CH:11][CH2:10][CH2:9]1)([O-:3])=[O:2]

Komponenten

5

Edukt 3

HCID 243Benzoic AcidHCID 31268PyrrolidineHCID 109429314-nitroheptanedial

Produkt 1

HCID 575067495-Nitrocyclohex-1-ene-1-carbaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 4-Nitro-heptanedial (35.2 g, 0.2 mol) in methylene chloride (0.7 L) were added pyrrolidine (2 ml, 0.024 mol) and benzoic acid (1.46 g, 0.012 mol), and the resulting mixture was refluxed for 10 to 15 hours. The reaction mixture was cooled to room temperature, washed with 1N HCl (170 ml), saturated with NaHCO3 (170 ml) and water (170 ml) and concentrated to give brownish oil with a purity of about 80%. The product was carried to the next step without further purification. Yield: 32.2 g, 75%. 1H NMR (400 MHz, CDCl3) δ 2.29-2.34 (m, 2H), 2.46-2.64 (m, 2H), 2.85-2.88 (m, 2H), 4.74 (m, 1H), 6.86 (m, 1H), 9.50 (s, 1H).

Aufarbeitung

  1. temperaturethe resulting mixture was refluxed for 10 to 15 hours
  2. washwashed with 1N HCl (170 ml), saturated with NaHCO3 (170 ml) and water (170 ml)
  3. concentrationconcentrated
  4. customto give brownish oil with a purity of about 80%
  5. customThe product was carried to the next step without further purification

Quellen und Nachweise

ORD-Eintrag
ord-1a017be3c45c4756b7b6a2b95a7e947a
Quelldatensatz
uspto-grants-2009_10
Patentnummer
US07605275B2

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