Sodium hydride → HCID 86644716、化合物

HRID 2407263ノート

反応式

HRID 2407263 の反応式
[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([OH:18])=[C:13]([C:15](=[O:17])[CH3:16])[CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].CC1C=CC(S(O[CH2:32][C@H:33]2[CH2:35][O:34]2)(=O)=O)=CC=1>CN(C=O)C>[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([O:18][CH2:32][C@H:33]2[CH2:35][O:34]2)=[C:13]([C:15](=[O:17])[CH3:16])[CH:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

5

実験手順

To a stirred solution of 1-(5-benzyloxy-2-hydroxyphenyl)ethanone (3.0 g, 12.4 mmol) in anhydrous DMF (15 ml) was added NaH (0.55 g, 13.6 mmol). The mixture was allowed to stir at RT for 30 min and then heated to 60° C. A solution of (R)-oxiran-2-ylmethyl 4-methylbenzenesulfonate (2.83 g, 12.4 mmol) in DMF was added dropwise at 60° C. during 1 h. Stirring was then continued at 60° C. for 3 h. The cooled reaction was quenched by addition of water (80 ml) and extracted three times with EtOAc. The combined organic layers were extracted twice with aq 1 M NaOH and washed with water and brine. The organic layer was dried with Na2SO4 and concentrated. The crude product obtained was purified by column chromatography with EtOAc/toluene as eluent to afford the title compound (2.35 g) as a white solid.

後処理

  1. temperatureheated to 60° C
  2. stirringStirring
  3. waitwas then continued at 60° C. for 3 h
  4. customThe cooled reaction
  5. customwas quenched by addition of water (80 ml)
  6. extractionextracted three times with EtOAc
  7. extractionThe combined organic layers were extracted twice with aq 1 M NaOH
  8. washwashed with water and brine
  9. dry with materialThe organic layer was dried with Na2SO4
  10. concentrationconcentrated
  11. customThe crude product obtained
  12. customwas purified by column chromatography with EtOAc/toluene as eluent

出典と根拠

ORDレコード
ord-3f5805e4c3fe47c78d3121f961372e21
出典データセット
uspto-grants-2014_08
特許番号
US08809536B2

反応ノート

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