Reaktion #1668702

ord-dc97a01aded549bf80d06e823c5e84ab

Reaktionsgleichung

[Na+].[OH-]
Sodium hydroxide
C=C1CNN(C(=O)OCc2ccccc2)C1
4-methylene-pyrazolidine-1-carboxylic acid 1-benzyl ester
O=C(Cl)Cc1ccc(F)cc1
(4-Fluorophenyl)acetyl chloride
C=C1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
desired product
Ausbeute 62.0%
C=C1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
2-[2-(4-fluorophenyl)acetyl]4-methylene-pyrazolidine-1-carboxylic acid benzyl ester
Ausbeute 62.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGto stir for 18 hours after which time the reaction mixture
  2. 2
    Sonstigeto separate
  3. 3
    ExtraktionThe aqueous layer is extracted with methylene chloride
  4. 4
    Sonstigedried
  5. 5
    Filtrationfiltered
  6. 6
    EinengenConcentration in vacuo
  7. 7
    Sonstigeaffords the crude product which
  8. 8
    Sonstigeis purified over silica (1:3 ethyl acetate/hexane)

Vorschrift

Sodium hydroxide (0.12 g, 3 mmol) is dissolved in a 1:2 water/methylene chloride solution (30 mL) with rapid stirring followed by the addition of 4-methylene-pyrazolidine-1-carboxylic acid 1-benzyl ester, 9, (0.62 g, 2.8 mmol) at room temperature. (4-Fluorophenyl)acetyl chloride (0.39 mL, 4.2 mmol) is added and the reaction is allowed to stir for 18 hours after which time the reaction mixture is diluted with water (10 mL) and the layers allowed to separate. The aqueous layer is extracted with methylene chloride, the organic layers combined, dried, and filtered. Concentration in vacuo affords the crude product which is purified over silica (1:3 ethyl acetate/hexane) to provide 0.54 g (62% yield) of the desired product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06730668B2uspto-grants-2004_05