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Hydrochloric Acid → 4-Chloro-2,3-dihydro-1H-isoindole

HRID 1630
ノート
印刷プレビュー

反応式

HRID 1630 の反応式
Cl[C:2]1[CH:3]=[C:4]2[C:9](=O)[NH:8][C:6](=O)[C:5]2=[CH:11][CH:12]=1.[ClH:13]>O1CCCC1>[Cl:13][C:11]1[CH:12]=[CH:2][CH:3]=[C:4]2[C:5]=1[CH2:6][NH:8][CH2:9]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 313Hydrochloric AcidHCID 2312394-Chloro-phthalimide

生成物 1

HCID 147958684-Chloro-2,3-dihydro-1H-isoindole

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 4-chlorophthalimide (60 g) in 1 liter of tetrahydrofuran was added borane-methyl sulfide complex (100 ml of 10M), and the mixture was refluxed overnight. After cooling, 100 ml of 6N hydrochloric acid was added slowly, the mixture refluxed for 2 hours, and then filtered. The filtrate was concentrated under reduced pressure, and the resulting aqueous solution washed with ethyl acetate. The aqueous layer was then basified with ammonium hydroxide and extracted with methylene chloride. Solvent was removed from the extract, and the residue distilled under vacuum to give 4-chloroisoindoline, a white solid, m.p. 48°-50° C.

後処理

  1. temperaturethe mixture was refluxed overnight
  2. temperatureAfter cooling
  3. temperaturethe mixture refluxed for 2 hours
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. washthe resulting aqueous solution washed with ethyl acetate
  7. extractionextracted with methylene chloride
  8. customSolvent was removed from the extract
  9. distillationthe residue distilled under vacuum

出典と根拠

ORDレコード
ord-9c7cc9bbc71144c7ae9f1e2d0e680324
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05726197

反応ノート

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