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2-Bromo-4-nitroanisole → 3-Bromo-4-methoxyaniline

HRID 19884
ノート
印刷プレビュー

反応式

HRID 19884 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[CH:4][C:3]=1[O:11][CH3:12]>C(O)C>[Br:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][C:3]=1[O:11][CH3:12]
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

3

反応物 1

HCID 788702-Bromo-4-nitroanisole

生成物 1

HCID 9610833-Bromo-4-methoxyaniline

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
70 °C

実験手順

Stannous chloride (96.839 g, 5.0 eq.) was added to a solution of 2-bromo-4-nitroanisole (23.7 g, 1.0 eq.) in ethanol (250 mL) and the mixture was stirred at 70° C. for 2 h, partitioned between ethyl acetate and sodium bicarbonate solution 10%. The pH was adjusted to 9 with 1N sodium hydroxide solution and the aqueous layer was extracted twice with ethyl acetate. The combined organic fractions were washed with water and brine, dried over magnesium sulfate, filtered, evaporated to dryness and purified on silica gel, eluting with hexane/ethyl acetate 1:1, to yield 13.82 g (67%) from the desired product as light brown solid. MS (m/e): 204.1 (MH+, 100%).

後処理

  1. custompartitioned between ethyl acetate and sodium bicarbonate solution 10%
  2. extractionthe aqueous layer was extracted twice with ethyl acetate
  3. washThe combined organic fractions were washed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated to dryness
  7. custompurified on silica gel
  8. washeluting with hexane/ethyl acetate 1:1

出典と根拠

ORDレコード
ord-f39bf865ebcb4bb39f868cb4430bed9f
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07745479B2

反応ノート

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