Hydrogen Peroxide → 1-(3,4,5-Trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(3-hydroxypropyl)-2-oxopyrrolidine

HRID 323497ノート

反応式

HRID 323497 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:24]=[C:25]([O:29][CH3:30])[C:26]=1[O:27][CH3:28])[CH2:6][N:7]1[CH2:11][CH2:10][C:9]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)([CH2:12][CH:13]=[CH2:14])[C:8]1=[O:23].C12BC(CCC1)CCC2.[OH-:40].[Na+].OO>O1CCCC1.CO.ClCCl>[CH3:30][O:29][C:25]1[CH:24]=[C:5]([CH:4]=[C:3]([O:2][CH3:1])[C:26]=1[O:27][CH3:28])[CH2:6][N:7]1[CH2:11][CH2:10][C:9]([CH2:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)([CH2:12][CH2:13][CH2:14][OH:40])[C:8]1=[O:23]

参加物

7

実験手順

Combine 1-(3,4,5-trimethoxybenzyl)-3-(4-fluorophenylmethyl)-3-(allyl)-2-oxopyrrolidine (0.677 g, 1.64 mmol) and tetrahydrofuran (10 mL). Add dropwise a solution of 9-BBN (9-borabicyclo[3.3.1]nonane) (5.56 mL, 0.5 M, 2.78 mmol) in tetrahydrofuran. After 1.5 hours, add dropwise an aqueous sodium hydroxide solution (10 mL, 1 M) and 30% aqueous hydrogen peroxide (1.5 mL, about 14.7 mmol). After 15 minutes heat the reaction mixture to reflux. After 1 hour, cool to ambient temperature, saturate the aqueous mixture with potassium carbonate and separate the layers. Extract the aqueous layer five times with diethyl ether. Combine the organic layers and dry over potassium carbonate, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 5% methanol/dichloromethane to give the title compound.

後処理

  1. temperatureAfter 15 minutes heat the reaction mixture
  2. temperatureto reflux
  3. waitAfter 1 hour
  4. concentrationsaturate the aqueous mixture with potassium carbonate
  5. customseparate the layers
  6. extractionExtract the aqueous layer five times with diethyl ether
  7. dry with materialdry over potassium carbonate
  8. filtrationfilter
  9. customevaporate in vacuo
  10. customto give a residue

出典と根拠

ORDレコード
ord-e0fe1c64531a4978b2bce8b2f5d10326
出典データセット
uspto-grants-2001_04
特許番号
US06211199B1

反応ノート

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