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Acetic Acid → N-Isopropyl-3-broMoaniline

HRID 365526
ノート
印刷プレビュー

反応式

HRID 365526 の反応式
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH:8]=[CH:9][CH:10]=1)[NH2:7].C(O)(=O)C.[CH3:15][C:16]([CH3:18])=O.C([O-])(=O)C.[Na+]>CCCCCC.CCOCC.O.C(O)C>[Br:3][C:4]1[CH:5]=[C:6]([NH:7][CH:16]([CH3:18])[CH3:15])[CH:8]=[CH:9][CH:10]=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

10

反応物 5

HCID 176Acetic AcidHCID 180AcetoneHCID 115623-BromoanilineHCID 517045Sodium AcetateHCID 4311764Sodium borohydride

生成物 1

HCID 23291934N-Isopropyl-3-broMoaniline

試薬・触媒・溶媒 4

HCID 702Ethanol
溶媒
HCID 962Water溶媒
HCID 3283Diethyl Ether溶媒
HCID 8058Hexane溶媒

反応条件

温度
0 °C

実験手順

Sodium borohydride (16.5 g, 435 mmol) was added slowly over 2 hours to a mixture of 3-bromoaniline (10 g, 58.13 mmol), ethanol (58 mL), acetic acid (50 mL, 866.1 mmol), water (140 mL), acetone (35 mL, 482.5 mmol), and sodium acetate (15.8 g, 116.2 mmol). The solution was stirred at 0° C. for 3 hours. The reaction mixture was poured into 1:1 mixture of ether and hexane containing 2N KOH. The layers were separated and the aqueous layer was extracted with ether/hexane (1:1). The combined organic layers were washed once with water and brine, dried with MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (10% ethyl acetate in hexane, Rf=0.31) to give the title compound (23.10 g, 93% as an oil:

後処理

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with ether/hexane (1:1)
  3. washThe combined organic layers were washed once with water and brine
  4. dry with materialdried with MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by silica gel chromatography (10% ethyl acetate in hexane, Rf=0.31)

出典と根拠

ORDレコード
ord-69262a77297e40e0ad93be9708005277
出典データセット
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06127382

反応ノート

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