Reacción #1861

ord-8fef71afc98949c49bc84e25d6876698

Ecuación de reacción

Cl.[Cl-].[Na+]
hydrochloric acid sodium chloride
C1CCC2=NCCCN2CC1
1,8-diazabicyclo[5.4.0]undec-7-ene
CCOC(=O)C[S+](C)C.[Br-]
carboethoxymethyl dimethylsulfonium bromide
O=C1C=CCC1
2-cyclopenten-1-one
CCOC(=O)C1C2CCC(=O)C21
title compound
Rendimiento 68.3%
CCOC(=O)C1C2CCC(=O)C21
(1SR,5RS,6SR) Ethyl 2-Oxobicyclo[3.1.0]hexane-6-carboxylate
Rendimiento 68.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter an additional 18 hours
  2. 2
    ExtracciónThe resulting mixture was extracted with diethyl ether
  3. 3
    SecadoThe combined ether extracts were dried over magnesium sulfate
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated in vacuo
  6. 6
    OtroThe residue was purified
  7. 7
    Lavadoeluting with a linear gradient of 10% ethyl acetate/hexanes to 50% ethyl acetate/hexanes

Procedimiento

A suspension of carboethoxymethyl dimethylsulfonium bromide (45.5 g) in toluene (350 mL) was treated with 1,8-diazabicyclo[5.4.0]undec-7-ene (30.2 g). The resulting mixture was stirred at room temperature. After one hour, the reaction mixture was treated with 2-cyclopenten-1-one (19.57 g). After an additional 18 hours, the reaction mixture was added to a 1N hydrochloric acid/sodium chloride solution. The resulting mixture was extracted with diethyl ether. The combined ether extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified using silica-gel chromatography, eluting with a linear gradient of 10% ethyl acetate/hexanes to 50% ethyl acetate/hexanes, to give 22.81 g of the title compound. Melting point: 36°-38° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726320uspto-grants-1998_03