Triethylamine → 3-Cyclopentyloxy-4-methoxybenzal hydantoin

HRID 582131

Reaktionsgleichung

Reaktionsgleichung von HRID 582131
CCOP(OCC)([CH:6]1[NH:12][C:10](=[O:11])[NH:9][C:7]1=[O:8])=O.C(N(CC)CC)C.[CH:23]1([O:28][C:29]2[CH:30]=[C:31]([CH:34]=[CH:35][C:36]=2[O:37][CH3:38])[CH:32]=O)[CH2:27][CH2:26][CH2:25][CH2:24]1>C(#N)C>[CH:23]1([O:28][C:29]2[CH:30]=[C:31]([CH:34]=[CH:35][C:36]=2[O:37][CH3:38])[CH:32]=[C:6]2[NH:12][C:10](=[O:11])[NH:9][C:7]2=[O:8])[CH2:24][CH2:25][CH2:26][CH2:27]1

Komponenten

5

Edukt 3

HCID 8471TriethylamineHCID 27358933-Cyclopentyloxy-4-methoxybenzaldehydeHCID 3516088Diethyl 5-hydantoylphosphonate

Produkt 1

HCID 543507273-Cyclopentyloxy-4-methoxybenzal hydantoinAusbeute 77,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel2×

Versuchsvorschrift

To a stirred solution of diethyl 5-hydantoylphosphonate (10 g, 42.3 mmol) and triethylamine (5.70 g, 56 mmol), in dry acetonitrile (100 ml) at room temperature was added a solution of 3-cyclopentyloxy-4-methoxybenzaldehyde (8 g, 36.3 mmol) in dry acetonitrile (75 ml), dropwise over 30 minutes. The resulting mixture was stirred at room temperature overnight, after which volatiles were removed in vacuo. The residue was diluted with 0.05N HCl (120 ml) and the precipitate collected by filtration. Recrystallization of this material with methylene chloride/methanol/diethyl ether afforded the title compound as a pale yellow solid (8.54 g). m.p. 220-222° C.

Aufarbeitung

  1. customafter which volatiles were removed in vacuo
  2. additionThe residue was diluted with 0.05N HCl (120 ml)
  3. filtrationthe precipitate collected by filtration
  4. customRecrystallization of this material with methylene chloride/methanol/diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-8002a67f5d7b458289c408796d875a7e
Quelldatensatz
uspto-grants-1999_07
Patentnummer
US05922751

Verknüpfte Notizen

Wird geladen…