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Methanol → HCID 67244427、化合物

HRID 2358377
ノート
印刷プレビュー

反応式

HRID 2358377 の反応式
[NH2:1][C:2]1[C:9]([CH3:10])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[I:11].CO>C1COCC1>[NH2:7][CH2:6][C:5]1[CH:8]=[C:9]([CH3:10])[C:2]([NH2:1])=[C:3]([I:11])[CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 887MethanolHCID 684571384-Amino-3-iodo-5-methyl-benzonitrile

生成物 1

HCID 67244427HCID 67244427、化合物収率 96.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

4-Amino-3-iodo-5-methylbenzonitrile (200 mg, 0.77 mmol) was dissolved in THF at 0° C. After Borane-THF complex (4 eq, 3.10 mmol, 3.10 ml) was slowly added into the reaction mixture, a reaction temperature was heated to reflux. The reaction mixture was stirred for 12 hr with reflux. After confirming the completion of the reaction, MeOH was added. The mixture was stirred for 4 hrs. The reaction solvent was removed in vacuo. A residue was extracted with Ethyl acetate, washed with H2O and brine, dried with Na2SO4 and concentrated in vacuo to yield 4-Aminomethyl-2-iodo-6-methyl-phenylamine (194 mg).

後処理

  1. additionAfter Borane-THF complex (4 eq, 3.10 mmol, 3.10 ml) was slowly added into the reaction mixture
  2. temperaturea reaction temperature was heated to reflux
  3. temperaturewith reflux
  4. additionwas added
  5. stirringThe mixture was stirred for 4 hrs
  6. customThe reaction solvent was removed in vacuo
  7. extractionA residue was extracted with Ethyl acetate
  8. washwashed with H2O and brine
  9. dry with materialdried with Na2SO4
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-7d2bbff9284541adacb438f8068f001c
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07763657B2

反応ノート

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