反応 #2319

ord-2f8da7ad30b2414dbbd1e045328ab620

反応方程式

COC(=O)CNC(=O)COc1ccc(C(C)=O)cc1
product
COC(=O)CNC(=O)COc1ccc(C(C)=O)cc1
methyl N-[4-(acetyl)-phenoxyacetyl]glycinate
O=C1CCC(=O)N1Br
N-bromosuccinimide
COC(=O)CNC(=O)COc1ccc(C(=O)CBr)cc1
methyl N-[4-(bromoacetyl)phenoxyacetyl]glycinate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux temperature for 64 hours
  2. 2
    その他The solvent was evaporated
  3. 3
    workup.DISSOLUTIONthe black residue dissolved in methanol/ethyl acetate
  4. 4
    workup.ADDITIONtreated with charcoal
  5. 5
    ろ過filtered
  6. 6
    その他evaporated
  7. 7
    その他The resulting brown oil was purified by flash chromatography on silica
  8. 8
    洗浄eluting with dichloromethane

実験手順

The product of step (i) (3.00 g) and N-bromosuccinimide (2.02 g) in carbon tetrachloride (50 ml) was heated at reflux temperature for 64 hours. The solvent was evaporated and the black residue dissolved in methanol/ethyl acetate, treated with charcoal, filtered and then evaporated. The resulting brown oil was purified by flash chromatography on silica, eluting with dichloromethane. Trituration with hexane gave methyl N-[4-(bromoacetyl)phenoxyacetyl]glycinate, 0.85 g, as a solid: mp softens 109°-111° C.; NMR (d6DMSO) δ 8.60 (1H, bt), 7.99 (2H, d), 7.09 (2H, d), 4.84 (2H, s), 4.69 (2H, s), 3.91 (2H, d), 3.64 (3H, s).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05728701uspto-grants-1998_03