Reaktion #44482

ord-0791347663924334bed116c48cda5629

Reaktionsgleichung

N#N
N2
CSC
DMS
C=CC(C(C)(C)O[SiH2]C(C)(C)C)C(C)(C)C(=O)OC
solution
C=CC(C(C)(C)O[SiH2]C(C)(C)C)C(C)(C)C(=O)OC
3-(tert-butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-pent-4-enoic acid methyl ester
CO
methanol
COC(=O)C(C)(C)C(C=O)C(C)(C)O[SiH2]C(C)(C)C
title compound
COC(=O)C(C)(C)C(C=O)C(C)(C)O[SiH2]C(C)(C)C
3-(tert-butyl-dimethyl-silanoxymethyl)-2,2-dimethyl-4-oxo-butyric acid methyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeO3 was bubbled for twenty-five minutes
  2. 2
    workup.ADDITIONwas added
  3. 3
    SonstigeThe solvent was evaporated in vacuo
  4. 4
    Sonstigethe product purified by flash column chromatography (hexanes:ethyl acetate) 100:0 to 50:50)

Vorschrift

A solution of Example 2C (3.5 g, 12.2 mmol)in dichloromethane (25 mL) and methanol (2.5 mL) was cooled to −78° C. and O3 was bubbled for twenty-five minutes. The reaction was purged with N2 and DMS (5.29 g, 85.4 mmol) was added. The reaction was stirred at room temperature for three hours. The solvent was evaporated in vacuo and the product purified by flash column chromatography (hexanes:ethyl acetate) 100:0 to 50:50) to provide the title compound as an oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737137B2uspto-grants-2010_06