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Sodium borohydride → 1-Methoxypiperidin-4-ol

HRID 1473783
ノート
印刷プレビュー

反応式

HRID 1473783 の反応式
[CH3:1][O:2][N:3]1[CH2:8][CH2:7][C:6](=[O:9])[CH2:5][CH2:4]1.[BH4-].[Na+]>C(O)C>[CH3:1][O:2][N:3]1[CH2:8][CH2:7][CH:6]([OH:9])[CH2:5][CH2:4]1
参加物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 4311764Sodium borohydrideHCID 199366531-Methoxypiperidin-4-one

生成物 1

HCID 30226061-Methoxypiperidin-4-ol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 1-methoxy-piperidin-4-one [prepared according to Journal of Organic Chemistry (1961), 26, 1867-74] (15.0 g, 116.1 mmol) in ethanol (430 ml) was added sodium borohydride 96% (2.29 g, 58.1 mmol) in portions. The reaction mixture was stirred at room temperature for 5 hours, evaporated to half of its volume, poured on cold saturated aqueous ammonium chloride and thoroughly extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (ethyl acetate). Yield: 10.9 g of 1-methoxy-piperidin-4-ol as a liquid.

後処理

  1. customevaporated to half of its volume
  2. additionpoured on cold saturated aqueous ammonium chloride
  3. extractionthoroughly extracted with ethyl acetate
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated
  7. customThe residue was purified by chromatography on silica gel (ethyl acetate)

出典と根拠

ORDレコード
ord-68199146adf349e895f22e1e5de378d0
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018135B2

反応ノート

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