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Stannous chloride dihydrate → 2-Amino-4-bromo-5-fluorophenol

HRID 1253931
ノート
印刷プレビュー

反応式

HRID 1253931 の反応式
O.O.[Sn](Cl)Cl.[Br:6][C:7]1[C:12]([F:13])=[CH:11][C:10]([OH:14])=[C:9]([N+:15]([O-])=O)[CH:8]=1>C(O)C>[NH2:15][C:9]1[CH:8]=[C:7]([Br:6])[C:12]([F:13])=[CH:11][C:10]=1[OH:14]
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

4

反応物 2

HCID 61436Stannous chloride dihydrateHCID 547590604-Bromo-5-fluoro-2-nitrophenol

生成物 1

HCID 383722992-Amino-4-bromo-5-fluorophenol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
85 °C

実験手順

Tin(II) chloride dihydrate (16.83 g, 74.6 mmol) was added to a solution of 4-bromo-5-fluoro-2-nitrophenol (4.4 g, 18.64 mmol) in ethanol (180 mL). The mixture was flushed with nitrogen and heated to 85° C. (oil bath temperature) for 1 day. The mixture was diluted with ethyl acetate (500 mL), saturated aqueous sodium bicarbonate (200 mL) was added with vigorous stirring. The mixture was filtered through celite and the celite pad was repeatedly washed with ethyl acetate. The two phases were separated and the organic phase was washed with brine. The combined aqueous phase was extracted with ethyl acetate. The combined organic phase was dried over MgSO4, filtered and concentrated to give 2-amino-4-bromo-5-fluorophenol. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.61 (br. s., 2H) 6.60 (d, J=10.11 Hz, 1H) 6.76 (d, J=7.33 Hz, 1H) 9.69 (br. s., 1 H).

後処理

  1. customThe mixture was flushed with nitrogen
  2. additionThe mixture was diluted with ethyl acetate (500 mL), saturated aqueous sodium bicarbonate (200 mL)
  3. additionwas added with vigorous stirring
  4. filtrationThe mixture was filtered through celite
  5. washthe celite pad was repeatedly washed with ethyl acetate
  6. customThe two phases were separated
  7. washthe organic phase was washed with brine
  8. extractionThe combined aqueous phase was extracted with ethyl acetate
  9. dry with materialThe combined organic phase was dried over MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-38db3c892cf74b92847489b3bffb93dd
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455522B2

反応ノート

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