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Hydrochloric Acid → HCID 19439673、化合物

HRID 1734018
ノート
印刷プレビュー

反応式

HRID 1734018 の反応式
O.NN.[C:4]([C:6]1[CH:7]=[C:8]([CH:21]=[CH:22][CH:23]=1)[CH2:9][N:10]1C(=O)C2=CC=CC=[C:12]2[C:11]1=[O:20])#[N:5].Cl>CO.O1CCCC1>[C:4]([C:6]1[CH:7]=[C:8]([CH:21]=[CH:22][CH:23]=1)[CH2:9][NH:10][C:11](=[O:20])[CH3:12])#[N:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 24654Hydrazine hydrate (1:1)HCID 123753363-((1,3-Dioxoisoindolin-2-yl)methyl)benzonitrile

生成物 1

HCID 19439673HCID 19439673、化合物収率 66%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of hydrazine hydrate (4.0 g) in methanol was added dropwise to a mixture of N-(3-cyanobenzyl)phthalimide (17.0 g) in tetrahydrofuran (150 ml) and methanol (120 ml) at ambient temperature under stirring and the resultant mixture was stirred for 3 hours at ambient temperature. To the reaction mixture was added dropwise 6N-hydrochloric acid (25 ml) and the mixture was stirred for one hour at ambient temperature. The reaction mixture was evaporated in vacuo. To the residue was added water (60 ml) and the mixture was stirred at 10 minutes and filtrated. The filtrate was washed with ethyl acetate and adjusted to pH 8.0 with 20% potassium carbonate solution. Acetic anhydride (15 ml) was added dropwise to the resulting solution at 8° to 20° C. under stirring and the mixture was stirred for one hour at 10° to 20° C. The reaction mixture was extracted with ethyl acetate, and extract was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was recrystallized from a mixture of ethyl acetate and diisopropyl ether to give N-(3-cyanobenzyl)acetamide (7.45 g).

後処理

  1. stirringthe mixture was stirred for one hour at ambient temperature
  2. customThe reaction mixture was evaporated in vacuo
  3. additionTo the residue was added water (60 ml)
  4. stirringthe mixture was stirred at 10 minutes
  5. filtrationfiltrated
  6. washThe filtrate was washed with ethyl acetate
  7. additionAcetic anhydride (15 ml) was added dropwise to the resulting solution at 8° to 20° C.
  8. stirringunder stirring
  9. stirringthe mixture was stirred for one hour at 10° to 20° C
  10. extractionThe reaction mixture was extracted with ethyl acetate
  11. extractionextract
  12. washwas washed with brine
  13. dry with materialdried over magnesium sulfate
  14. customThe solvent was evaporated in vacuo
  15. customthe residue was recrystallized from a mixture of ethyl acetate and diisopropyl ether

出典と根拠

ORDレコード
ord-58480338e0874a3b81c5d0453c97a24e
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05532258

反応ノート

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