Sodium borohydride → 1-(6-Bromopyridin-2-yl)ethane-1,2-diol

HRID 385808ノート

反応式

HRID 385808 の反応式
[Br:1][C:2]1[N:7]=[C:6]([C:8](=[O:11])[CH2:9][OH:10])[CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>C(O)C>[Br:1][C:2]1[N:7]=[C:6]([CH:8]([OH:11])[CH2:9][OH:10])[CH:5]=[CH:4][CH:3]=1

参加物

4

実験手順

A solution of 1-(6-bromopyridin-2-yl)-2-hydroxyethanone (2.2 g, 10.18 mmol) in ethanol (127 mL) was charged with sodium borohydride (0.385 g, 10.18 mmol). After 30 minutes, the reaction was concentrated to dryness and then partitioned between ethyl acetate (50 mL) and 3:1 saturated aqueous sodium bicarbonate:water (25 mL). The layers were separated and the organic layer was washed with brine (25 mL), dried over sodium sulfate, filtered, and concentrated to afford the title compound. 1H NMR (600 MHz, DMSO): δ 7.69 (m, 1H), 7.46 (m, 2H), 5.50 (d, J=5.0 Hz, 1H), 4.69 (m, 1H), 4.49 (m, 1H), 3.61 (m, 1H), 3.46 (m, 1H).

後処理

  1. concentrationthe reaction was concentrated to dryness
  2. custompartitioned between ethyl acetate (50 mL) and 3:1 saturated aqueous sodium bicarbonate
  3. customThe layers were separated
  4. washthe organic layer was washed with brine (25 mL)
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-2bf238c9c0ec4e1da4fa1f40b9c79a50
出典データセット
uspto-grants-2013_02
特許番号
US08367706B2

反応ノート

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