Formaldehyde → 1-(4-Chlorobenzyl)-3-hydroxymethyl-3-methyl-2-oxocyclopentanecarboxylic acid methyl ester

HRID 873509Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 873509
C=O.[C:3](=O)([O-])[O-:4].[K+].[K+].[CH3:9][O:10][C:11]([C:13]1([CH2:20][C:21]2[CH:26]=[CH:25][C:24]([Cl:27])=[CH:23][CH:22]=2)[CH2:17][CH2:16][CH:15]([CH3:18])[C:14]1=[O:19])=[O:12]>O>[CH3:9][O:10][C:11]([C:13]1([CH2:20][C:21]2[CH:22]=[CH:23][C:24]([Cl:27])=[CH:25][CH:26]=2)[CH2:17][CH2:16][C:15]([CH2:3][OH:4])([CH3:18])[C:14]1=[O:19])=[O:12]

Komponenten

5

Versuchsvorschrift

A 37% formaldehyde aqueous solution (0.90 ml) and potassium carbonate (2.00 mmol) were added to 1-(4-chlorobenzyl)-3-methyl-2-oxocyclopentanecarboxylic acid methyl ester (Compound VIII-1) (4.00 mmol), and the resultant mixture was stirred at room temperature for 4 hours. After the reaction, water was added to the resultant reaction solution, and the solution was extracted with ethyl acetate. The organic layer was washed with saturated brine, and thereafter dried over anhydrous sodium sulfate. The solvent was distilled off, and a residue was purified with the use of a silica gel column. In this way, Compound VII-1 in the form of two isomers (isomer VII-1a and isomer VII-1b) was obtained. Note that Compound VIII-1 was synthesized in accordance with a method described in Patent Literature 1.

Aufarbeitung

  1. additionwas added to the resultant
  2. customreaction solution
  3. extractionthe solution was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationThe solvent was distilled off
  7. customa residue was purified with the use of a silica gel column
  8. customIn this way, Compound VII-1 in the form of two isomers (isomer VII-1a and isomer VII-1b) was obtained
  9. customwas synthesized in accordance with a method

Quellen und Nachweise

ORD-Eintrag
ord-6141951a41ba40f2aeb549412c2eabb3
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08975434B2

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