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Hydrochloric Acid → HCID 19439673, 화합물

HRID 1734018
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HRID 1734018 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

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

생성물 1

HCID 19439673HCID 19439673, 화합물수율 66%

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 8028Tetrahydrofuran
용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-58480338e0874a3b81c5d0453c97a24e
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05532258

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