Potassium;tri(butan-2-yl)boranuide → (3SR,4SR)-1,4-dibenzyl-piperidin-3-ol

HRID 382789ノート

反応式

HRID 382789 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:10](=[O:21])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCC(C)[BH-](C(C)CC)C(C)CC.[K+]>C1COCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:10]([OH:21])[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

4

反応条件

温度
-70 °C

実験手順

To a solution of 9.0 g (SR)-1,4-dibenzyl-piperidin-3-one (32 mmol) in 200 ml dry THF were added at −78° C. dropwise 48 ml K-selectride® (1 N in THF, 48 mmol). The reaction mixture was stirred for 1 h at −70° C. and then warmed to r.t. The reaction was quenched by the addition of 100 ml NaHCO3-solution and the aqueous phase was extracted twice with ethyl acetate (200 ml). The combined organic phases were washed with water (100 ml) and brine (100 ml). The organic phase was dried over MgSO4, filtrated and the solvent was removed under reduced pressure to give the crude product. Purification by chromatography (ethyl acetate/hexane 1/2 to 2/1) yielded 6.5 g of the product (23 mmol, 72%) as a yellow oil.

後処理

  1. temperaturewarmed to r.t
  2. customThe reaction was quenched by the addition of 100 ml NaHCO3-solution
  3. extractionthe aqueous phase was extracted twice with ethyl acetate (200 ml)
  4. washThe combined organic phases were washed with water (100 ml) and brine (100 ml)
  5. dry with materialThe organic phase was dried over MgSO4
  6. filtrationfiltrated
  7. customthe solvent was removed under reduced pressure
  8. customto give the crude product
  9. customPurification by chromatography (ethyl acetate/hexane 1/2 to 2/1)

出典と根拠

ORDレコード
ord-9ad44e8221694e9dad8e8084c18a3b6d
出典データセット
uspto-grants-2001_10
特許番号
US06310213B1

反応ノート

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