反応 #48323

ord-b4ede3342f58419b9e8e391148d5fd35

反応方程式

C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)C
crude material
C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)C
Tert-butyl (2S,3S)-1-(allyloxy)-3-(tert-butyldimethylsilyloxy)-4-hydroxybutan-2-ylcarbamate
CC(=O)OI1(OC(C)=O)(OC(C)=O)OC(=O)c2ccccc21
Dess-Martin periodinane
C=CCOC[C@H](NC(=O)OC(C)(C)C)[C@@H](C=O)O[Si](C)(C)C(C)(C)C
Tert-butyl (2S,3S)-1-(allyloxy)-3-(tert-butyldimethylsilyloxy)-4-oxobutan-2-ylcarbamate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe biphasic mixture was stirred until it
  2. 2
    洗浄The organic layer was washed with brine
  3. 3
    乾燥dried (Na2SO4)
  4. 4
    ろ過filtered
  5. 5
    その他The crude aldehyde was used without further purification

実験手順

The crude material from Step 4 (0.040 g) was dissolved in CH2Cl2 (3 mL) and treated with Dess-Martin periodinane (0.07 g, 0.2 mmol). The mixture was stirred at ambient temperature for 4 h then diluted with EtOAc (10 mL), sat'd NaHCO3 (5 mL), and aqueous Na2S2O3 (5 mL). The biphasic mixture was stirred until it was colorless. The organic layer was washed with brine, dried (Na2SO4), filtered, and conc in vacuo. The crude aldehyde was used without further purification.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07745484B2uspto-grants-2010_06