反応 #2006485

ord-d66d4fc880b54ab3afc0ceda0eee8bed

反応方程式

O=S(=O)([O-])[O-].[Na+].[Na+]
sodium sulphate
COC(=O)CC1(O)CCN(Cc2ccccc2)CC1
compound 24
COC(=O)CC1(O)CCN(Cc2ccccc2)CC1
(1-Benzyl-4-hydroxy-piperidin-4-yl)-acetic acid methyl ester
[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminium hydride
OCCC1(O)CCN(Cc2ccccc2)CC1
crude compound 25
収率 92.4%
OCCC1(O)CCN(Cc2ccccc2)CC1
1-Benzyl-4-(2-hydroxy-ethyl)-piperidin-4-ol
収率 92.4%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to return to room temperature
  2. 2
    workup.STIRRINGto be stirred for an additional 2 hrs
  3. 3
    抽出extracted with diethyl ether (3×75 mL)
  4. 4
    洗浄washed with brine
  5. 5
    乾燥finally dried over magnesium sulphate

実験手順

To a solution of compound 24 (1.70 g, 6.07 mmol) in anhydrous THF (40 mL) at 0° C. was slowly added a solution of lithium aluminium hydride (1.0M in THF) (12.1 mL, 12.1 mmol). The solution was then stirred at 0° C. for 1 hr and allowed to return to room temperature to be stirred for an additional 2 hrs. The resulting solution was poured in a cold 10% solution of sodium sulphate (300 mL), extracted with diethyl ether (3×75 mL), washed with brine and finally dried over magnesium sulphate to give the crude compound 25 (1.32 g, 87%) which was used as such in the next step. 1H NMR (400 MHz, MeOD) δ: 1.65 (m, 4H), 1.72 (t, 2H, J=7.06 Hz), 2.45 (m, 2H), 2.62 (m, 2H), 3.56 (s, 2H), 3.76 (t, 2H, J=7.06 Hz), 7.31 (m, 5H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08168627B2uspto-grants-2012_05