Reaktion #1853138
ord-8333149159a34a1c9f630e14f198549d
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONthe base added
- 2Sonstigethe flask was kept in an ice bath
- 3Sonstigeto get to room temperature
- 4Sonstigewas removed
- 5workup.DISSOLUTIONthe raw mixture was dissolved in CH2Cl2
- 6ExtraktionAfter extraction with water the organic layer
- 7Sonstigethe monomer was separated by purification on a silica column
- 8SonstigeThe overall reaction scheme
- 9Sonstigefor preparation of them monomer
- 10Sonstigeis illustrated in Reaction Scheme I
Vorschrift
The reaction is based on that described by Whitcombe et al (J Am Chem Soc 117, 7105–7111 (1995)); the molar ratios were choroformate:vinylphenol: diisopropylethylamine 1:1.2. The vinylphenol was dissolved in dry THF and the base added; the flask was kept in an ice bath an the chlorformate added dropwise; the flask was allowed to get to room temperature and the reaction was monitored (TLC 60–40 cyclohexane-dichloromethane)), the solvent was removed and the raw mixture was dissolved in CH2Cl2. After extraction with water the organic layer was taken down to dryness and the monomer was separated by purification on a silica column using a stepwise gradient of CH2Cl2-hexane (from 5% CH2Cl2 to 80%). The analysis showed purity >98%. The overall reaction scheme for preparation of them monomer is illustrated in Reaction Scheme I.