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1-(2-Methyl-1-propenyl)-3-nitrobenzene → 3-Isobutylaniline

HRID 249141
ノート
印刷プレビュー

反応式

HRID 249141 の反応式
[CH3:1][C:2]([CH3:13])=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([N+:10]([O-])=O)[CH:5]=1>CO.Cl.[Pd]>[CH2:3]([C:4]1[CH:5]=[C:6]([NH2:10])[CH:7]=[CH:8][CH:9]=1)[CH:2]([CH3:13])[CH3:1]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 118161771-(2-Methyl-1-propenyl)-3-nitrobenzene

生成物 1

HCID 190247993-Isobutylaniline収率 103.4%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 313Hydrochloric Acid溶媒HCID 887Methanol溶媒

反応条件

温度
25 °C

実験手順

To a solution of 1-(2-methyl-1-propenyl)-3-nitrobenzene (4.57 g) in a mixture of methanol (50 ml) and 6N hydrochloric acid (14 ml) was added 10% palladium on activated carbon (1 g), and the mixture was stirred under hydrogen atmosphere (3 atm) at 25° C. for 3 hours. The catalyst was filtered off, and the filtrate was evaporated. The residue was poured into a mixture of ethyl acetate and aqueous sodium bicarbonate. The organic layer was separated, washed with water and brine, and dried over magnesium sulfate. Evaporation of the solvent gave 3-isobutylphenylamine (3.98 g) as a brown oil.

後処理

  1. filtrationThe catalyst was filtered off
  2. customthe filtrate was evaporated
  3. additionThe residue was poured into a mixture of ethyl acetate and aqueous sodium bicarbonate
  4. customThe organic layer was separated
  5. washwashed with water and brine
  6. dry with materialdried over magnesium sulfate
  7. customEvaporation of the solvent

出典と根拠

ORDレコード
ord-2564850177c84120a6750dffd2d101d7
出典データセット
uspto-grants-1993_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05212320

反応ノート

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