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Stannous chloride dihydrate → 3-Amino-5-bromobenzonitrile

HRID 2071036
ノート
印刷プレビュー

反応式

HRID 2071036 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

HCID 534069613-Amino-5-bromobenzonitrile収率 63%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-bab4d3d1873f4be6818cbc4943a3d653
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08299267B2

反応ノート

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