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Acetic Acid → 4-Bromo-3-chloro-5-methylaniline

HRID 1755011
ノート
印刷プレビュー

反応式

HRID 1755011 の反応式
C(O)(=O)C.[Br:5][C:6]1[C:11]([CH3:12])=[CH:10][C:9]([N+:13]([O-])=O)=[CH:8][C:7]=1[Cl:16].O.C(=O)(O)[O-].[Na+]>C(O)C.[Fe]>[Br:5][C:6]1[C:11]([CH3:12])=[CH:10][C:9]([NH2:13])=[CH:8][C:7]=1[Cl:16]
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

7

反応物 4

HCID 176Acetic AcidHCID 962WaterHCID 516892Sodium BicarbonateHCID 218863692-Bromo-1-chloro-3-methyl-5-nitrobenzene

生成物 1

HCID 668171834-Bromo-3-chloro-5-methylaniline収率 98%

試薬・触媒・溶媒 2

HCID 23925Iron触媒
HCID 702
Ethanol
溶媒

反応条件

温度
100 °C

実験手順

Iron (2.34 g, 41.8 mmol) and acetic acid (0.80 mL, 14.0 mmol) were added to a mixed solution of 2-bromo-1-chloro-3-methyl-5-nitro-benzene (3.50 g, 14.0 mmol) in ethanol (15 mL)-water (31 mL) at room temperature. The mixture was stirred at 100° C. for one hour, and a saturated aqueous sodium bicarbonate solution was then added at 0° C. The mixture was filtered through celite, and the filtrate was washed with ethyl acetate and water. The filtrate was concentrated under reduced pressure. Ethyl acetate was then added, and the organic layer and the aqueous layer were separated. The aqueous layer was repeatedly extracted with ethyl acetate three times, and the organic layers were then dried over sodium sulfate. The resulting residue was concentrated under reduced pressure to give 4-bromo-3-chloro-5-methyl-phenylamine as a pale brown solid (3.01 g, 98%).

後処理

  1. filtrationThe mixture was filtered through celite
  2. washthe filtrate was washed with ethyl acetate and water
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. additionEthyl acetate was then added
  5. customthe organic layer and the aqueous layer were separated
  6. extractionThe aqueous layer was repeatedly extracted with ethyl acetate three times
  7. dry with materialthe organic layers were then dried over sodium sulfate
  8. concentrationThe resulting residue was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-2282d8a8bb24435a8e0969d8d7e249a5
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09169254B2

反応ノート

読み込み中…

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