反応 #2244

ord-45b51dfa48a4401f8cc762580c573748

反応方程式

Cn1c(C=Cc2ccccc2O)cc2ccccc21
2-[2-(2-hydroxyphenyl)vinyl]-1-methylindole
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOC(=O)/N=N/C(=O)OCC
diethylazodicarboxylate
C1CCOC1
THF
COC(=O)[C@H](C)Oc1ccccc1C=Cc1cc2ccccc2n1C
(S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole
収率 90.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled condition
  2. 2
    抽出followed by extraction with methylene chloride
  3. 3
    乾燥The extract was dried over Na2SO4
  4. 4
    その他evaporated
  5. 5
    workup.ADDITIONCHCl3 -n-hexane was added to the residue
  6. 6
    ろ過after filtration
  7. 7
    その他the organic layer was purified by silica gel column chromatography (CHCl3 /n-hexane/AcOEt=10/10/1)

実験手順

To a solution of 1.50 g (6.02 mmol) of 2-[2-(2-hydroxyphenyl)vinyl]-1-methylindole, 1.89 g (7.21 mmol) of triphenylphosphine and 0.69 ml (7.22 mmol) of R-(+)-methyl lactate in 15 ml of THF was added 1.14 ml (7.24 mmol) of diethylazodicarboxylate under an ice-cooled condition, followed by stirring at room temperature for 2 hours. Brine was added to the reaction mixture, followed by extraction with methylene chloride. The extract was dried over Na2SO4, and evaporated. CHCl3 -n-hexane was added to the residue and, after filtration, the organic layer was purified by silica gel column chromatography (CHCl3 /n-hexane/AcOEt=10/10/1) to give 1.82 g (90%) of (S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05728709uspto-grants-1998_03