Réaction #44482

ord-0791347663924334bed116c48cda5629

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreO3 was bubbled for twenty-five minutes
  2. 2
    workup.ADDITIONwas added
  3. 3
    AutreThe solvent was evaporated in vacuo
  4. 4
    Autrethe product purified by flash column chromatography (hexanes:ethyl acetate) 100:0 to 50:50)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07737137B2uspto-grants-2010_06