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Stannous chloride dihydrate → 3-Amino-5-bromobenzonitrile

HRID 2071036
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HRID 2071036 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:10]([O-])=O)[CH:9]=1)[C:5]#[N:6].O.O.Cl[Sn]Cl>C1COCC1.CCO>[NH2:10][C:8]1[CH:7]=[C:4]([CH:3]=[C:2]([Br:1])[CH:9]=1)[C:5]#[N:6]
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참가 물질

5

반응물 2

HCID 61436Stannous chloride dihydrateHCID 51524253-Bromo-5-nitrobenzonitrile

생성물 1

HCID 534069613-Amino-5-bromobenzonitrile수율 63%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a stirring solution of 845 mg (3.72 mmol) of 3-bromo-5-nitrobenzonitrile in 5 mL of THF and 5 mL of EtOH was added 4.2 g (18.6 mmol) of SnCl2.2H2O in several portions. The reaction became slightly exothermic and was stirred at r.t. for about 12.5 h. The mixture was concentrated and 30 mL of 2 N NaOH was added. After the mixture was stirred for 2 h, H2O and EtOAc were added, and the organic layer was washed with 50 mL of H2O and 40 mL of brine. The aqueous layer was extracted with EtOAc and washed with brine. The combined extracts were dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (35% EtOAc/hexanes) provided 461 mg of 3-amino-5-bromobenzonitrile as a yellow solid in 63% yield.

후처리

  1. concentrationThe mixture was concentrated
  2. addition30 mL of 2 N NaOH was added
  3. stirringAfter the mixture was stirred for 2 h
  4. additionH2O and EtOAc were added
  5. washthe organic layer was washed with 50 mL of H2O and 40 mL of brine
  6. extractionThe aqueous layer was extracted with EtOAc
  7. washwashed with brine
  8. dry with materialThe combined extracts were dried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customPurification by flash silica gel chromatography (35% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-bab4d3d1873f4be6818cbc4943a3d653
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299267B2

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