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Ammonium Hydroxide → 1-(3-Cyanophenyl)urea

HRID 272781
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HRID 272781 반응식
[C:1]([C:3]1[CH:4]=[C:5]([N:9]=[C:10]=[O:11])[CH:6]=[CH:7][CH:8]=1)#[N:2].[OH-].[NH4+:13]>C1COCC1>[C:1]([C:3]1[CH:4]=[C:5]([NH:9][C:10]([NH2:13])=[O:11])[CH:6]=[CH:7][CH:8]=1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 27333153-Isocyanatobenzonitrile

생성물 1

HCID 206364711-(3-Cyanophenyl)urea

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To 3-cyanophenyl isocyanate (1.0 g, 6.90 mmol) in THF (5 mL), ammonium hydroxide (1.7 mL, 13.8 mmol) was added. The reaction was stirred for 2 h at rt. The solvent was evaporated and the crude residue was redissolved in ethyl acetate. The organic layer was washed with water and brine and dried over sodium sulfate. The solvent was evaporated and the crude residue was purified by flash column chromatography to 41A (0.37 g).

후처리

  1. customThe solvent was evaporated
  2. dissolutionthe crude residue was redissolved in ethyl acetate
  3. washThe organic layer was washed with water and brine
  4. dry with materialdried over sodium sulfate
  5. customThe solvent was evaporated
  6. customthe crude residue was purified by flash column chromatography to 41A (0.37 g)

출처 및 근거

ORD 기록
ord-cc36db0608964e15b7d2f4c53ebf0783
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07456195B2

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