Reacción #696701

ord-4daad2cc5fc248529c67dc5501cbe798

Ecuación de reacción

CCC1Cc2c(-c3ccccc3)cccc2C1O
2-ethyl-1-hydroxy-4-phenylindan
CCN(CC)CC
triethylamine
CS(=O)(=O)Cl
methanesulfonyl chloride
CCC1=Cc2c(cccc2-c2ccccc2)C1
aimed product
Rendimiento 72.1%
CCC1=Cc2c(cccc2-c2ccccc2)C1
2-ethyl-4-phenylindene
Rendimiento 72.1%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroTo a 300-ml four-necked round flask (equipped with a stirrer tip, a dropping funnel
  2. 2
    workup.ADDITIONAfter the dropwise addition
  3. 3
    Otrothe organic phase was separated
  4. 4
    Extracciónthe aqueous phase was extracted twice with 50 ml of methylene chloride
  5. 5
    LavadoThe combined organic phases were washed with a saturated NaHCO3 aqueous solution
  6. 6
    Secadoby drying over anhydrous Na2SO4
  7. 7
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  8. 8
    Otrothe residue was purified by silica gel chromatography

Procedimiento

To a 300-ml four-necked round flask (equipped with a stirrer tip, a dropping funnel and a thermometer) were introduced 9.78 g (41.3 mmol) of 2-ethyl-1-hydroxy-4-phenylindan, 17.2 ml (123.8 mmol) of triethylamine, 0.25 g (2.1 mmol) of 4-dimethylaminopyridine and 98 ml of methylene chloride, and then in a nitrogen atmosphere under ice cooling, a solution of 6.4 ml (82.5 mmol) of methanesulfonyl chloride in 6.5 ml of methylene chloride was dropwise added slowly. After the dropwise addition was completed, the reaction was performed for further 3.5 hours at the same temperature. The reaction mixture was poured into 250 ml of ice water, the organic phase was separated, and the aqueous phase was extracted twice with 50 ml of methylene chloride. The combined organic phases were washed with a saturated NaHCO3 aqueous solution and then with a saturated saline solution, followed by drying over anhydrous Na2SO4. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel chromatography using hexane to obtain 6.56 g of the aimed product (a mixture of isomers) as a light yellow liquid (yield: 73%). The properties of the product thus obtained are described below.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05998039uspto-grants-1999_12