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Trichloroacetic Acid → 3,4-dihydro-5-methyl-1(2H)-isoquinolinone

HRID 1645906
ノート
印刷プレビュー

反応式

HRID 1645906 の反応式
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:11].ClC(Cl)(Cl)C(O)=O.[N-:19]=[N+]=[N-].[Na+]>>[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH2:4][CH2:5][NH:19][C:6]2=[O:11]
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 3

HCID 6421Trichloroacetic AcidHCID 33557Sodium Azide2 回HCID 44184314-Methyl-1-indanone

生成物 1

HCID 1481403,4-dihydro-5-methyl-1(2H)-isoquinolinone収率 47.2%

実験手順

A mixture of 4.7 g (32.2 mmol) of 2,3-dihydro-4-methyl-1H-inden-1-one and 53 g of trichloroacetic acid was heated to 65°. To the resulting solution was added 4.2 g (64.4 mmol) of sodium azide and the mixture was kept at 65° for 18 hours. An additional 1.0 g of sodium azide was then added and heating continued for another four hours. The mixture was diluted with 200 ml of ice water and extracted with ether. The ether extracts were washed with water, saturated sodium hydrogen carbonate, dried (MgSO4), and concentrated. The residue was chromatographed (SiO2, ether to ether/methanol 95/5). The resulting product was recrystallized from toluene to give 2.45 g (47%) of product; mp 141°-143°.

後処理

  1. temperaturewas heated to 65°
  2. temperatureheating
  3. waitcontinued for another four hours
  4. extractionextracted with ether
  5. washThe ether extracts were washed with water, saturated sodium hydrogen carbonate
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. customThe residue was chromatographed (SiO2, ether to ether/methanol 95/5)
  9. customThe resulting product was recrystallized from toluene

出典と根拠

ORDレコード
ord-004b3a8eb7984ec59b486de9877e9986
出典データセット
uspto-grants-1993_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05177075

反応ノート

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