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Ethanol → 5-Methyl-2,3-dihydro-1H-isoindol-1-one

HRID 1454280
ノート
印刷プレビュー

反応式

HRID 1454280 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[N:6](CC=CC1C=CC=CC=1)[CH2:5]2.C(O)C>CCCCCC.C(OCC)(=O)C>[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[NH:6][CH2:5]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 702EthanolHCID 68567766HCID 68567766、化合物

生成物 1

HCID 220646715-Methyl-2,3-dihydro-1H-isoindol-1-one

試薬・触媒・溶媒 1

HCID 21226206Ethyl acetate hexane溶媒

実験手順

5-Methyl-2-(phenyl-allyl)-2,3-dihydro-isoindol-1-one (3.64 g, 14.61 mmol) was taken up in a 50/50 mixture of ethanol-3M HCl (100 mL) and heated to 80EC for 12 h. The reaction mixture was cooled and the ethanol was removed under reduced pressure. The aqueous layer was extracted three times with ethyl acetate and the combined organic layers were washed with water, brine and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The product was isolated by flash chromatography. (1:1 hexane/ethyl acetate) Yield 1.40 g. 1H NMR (CDCl3, 300 MHz): δ 2.51 (s, 3H), 4.48 9s, 2H), 7.27-7.36 (m, 2H), 7.75 (d, J=8 Hz, 1H).

後処理

  1. temperatureheated to 80EC for 12 h
  2. temperatureThe reaction mixture was cooled
  3. customthe ethanol was removed under reduced pressure
  4. extractionThe aqueous layer was extracted three times with ethyl acetate
  5. washthe combined organic layers were washed with water, brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationThe solution was filtered
  8. customthe solvent removed under reduced pressure
  9. customThe product was isolated by flash chromatography

出典と根拠

ORDレコード
ord-e000b96a640b43888464a0a8d008eee0
出典データセット
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07479495B2

反応ノート

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