Phthaloyl chloride → Methyl 2-fluoromethyl-2-phthalimido-4-pentenoate

HRID 1995578Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1995578
[F:1][CH2:2][C:3]([NH2:11])([CH2:8][CH:9]=[CH2:10])[C:4]([O:6][CH3:7])=[O:5].C(N(CC)CC)C.[C:19](Cl)(=[O:29])[C:20]1[C:21](=[CH:25][CH:26]=[CH:27][CH:28]=1)[C:22](Cl)=[O:23].C1(=O)NC(=O)C2=CC=CC1=C2>ClCCl>[F:1][CH2:2][C:3]([N:11]1[C:22](=[O:23])[C:21]2=[CH:25][CH:26]=[CH:27][CH:28]=[C:20]2[C:19]1=[O:29])([CH2:8][CH:9]=[CH2:10])[C:4]([O:6][CH3:7])=[O:5]

Komponenten

6

Versuchsvorschrift

To a solution of methyl 2-fluoromethyl-2-amino-4-pentenoate (2.10 g, 13 mmol) and triethylamine (3 g) in dry dichloromethane, phthaloyl dichloride (2.37 g, 11.7 mmol) is added with ice cooling. After stirring overnight, at room temperature, the solution is washed with water and 1 N HCl. Drying and removal of solvent by evaporation gives a residue, consisting mainly of the iso-phthalimide. The residue is dissolved in dry dichloromethane, two equivalents of triethylamine are added, and the mixture is refluxed overnight. Work-up as described above gives the title compound as an oil (3.0 g).

Aufarbeitung

  1. washthe solution is washed with water and 1 N HCl
  2. customDrying
  3. customremoval of solvent
  4. customby evaporation
  5. customgives a residue
  6. temperaturethe mixture is refluxed overnight

Quellen und Nachweise

ORD-Eintrag
ord-38a170fca28d48518fd0a926522659b6
Quelldatensatz
uspto-grants-1983_09
Patentnummer
US04405530

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