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Sodium Hydroxide → 3,5-Diaminobenzonitrile

HRID 1190897
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HRID 1190897 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([N+:12]([O-])=O)[CH:11]=1)[C:7]#[N:8])([O-])=O.Cl[Sn]Cl.[OH-].[Na+]>Cl>[NH2:1][C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([NH2:12])[CH:11]=1)[C:7]#[N:8]
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 200623,5-DinitrobenzonitrileHCID 24479Stannous Chloride

생성물 1

HCID 128973293,5-Diaminobenzonitrile수율 57%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

To 3,5-dinitrobenzonitrile (5.0 g, 25.89 mmol) in 20 mL of HCl 1M, was added SnCl2 (34.4 g, 7 eq). The reaction mixture was stirred at room temperature for 2 h and then cooled to 0° C. The mixture was made alkaline with a 50% aqueous solution of NaOH and the precipitate was removed by filtration. The filtrate was extracted with ethyl acetate and the combined organic layers were evaporated. The residue and the precipitate were purified by flash chromatography on silica gel (DCM/MeOH//95/5) to yield expected compound as an orange solid (1.95 g, 57% yield). m/z (ESI) 134.0 [M+H]+.

후처리

  1. temperaturecooled to 0° C
  2. customthe precipitate was removed by filtration
  3. extractionThe filtrate was extracted with ethyl acetate
  4. customthe combined organic layers were evaporated
  5. customThe residue and the precipitate were purified by flash chromatography on silica gel (DCM/MeOH//95/5)

출처 및 근거

ORD 기록
ord-c9d06e2ce5ab4de282e6822838a95cc4
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680095B2

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