Acetic Acid → Ammonia

HRID 225767

反応式

HRID 225767 の反応式
[OH:1][CH:2]1[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.[CH3:8][C:9]([CH3:11])=O.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>O1CCCC1>[NH3:5].[CH:9]([N:5]1[CH2:6][CH2:7][CH:2]([OH:1])[CH2:3][CH2:4]1)([CH3:11])[CH3:8]

参加物

7

実験手順

A mixture of 4-hydroxypiperidine (10 g, 0.10 mol), acetone (21.8 mL, 0.30 mol), acetic acid (5.7 mL, 0.10 mol) and tetrahydrofuran (150 mL) was stirred in an ice bath for 15 minutes. Sodium triacetoxyborohydride (31.3 g, 0.15mol) was then added portionwise and the mixture was stirred for a further 10 minutes. The reaction mixture was then warmed and stirred at room temperature for 10 minutes and at 40° C. for 2.5 hours. The solvent was evaporated under reduced pressure and the residue was dissolved in water (50 mL). The aqueous solution was basified to pH9 with 0.88 ammonia and the solution was stirred for 30 minutes. The reaction mixture was then extracted with diethyl ether (2×200 mL) and the combined extracts were dried over sodium sulfate and concentrated in vacuo to give a yellow oil. The oil was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 96:4:1 to 90:10:1, to afford the title product as a yellow oil in quantitative yield, 14.6 g.

後処理

  1. stirringthe mixture was stirred for a further 10 minutes
  2. temperatureThe reaction mixture was then warmed
  3. stirringstirred at room temperature for 10 minutes and at 40° C. for 2.5 hours
  4. customThe solvent was evaporated under reduced pressure
  5. dissolutionthe residue was dissolved in water (50 mL)
  6. stirringthe solution was stirred for 30 minutes
  7. extractionThe reaction mixture was then extracted with diethyl ether (2×200 mL)
  8. dry with materialthe combined extracts were dried over sodium sulfate
  9. concentrationconcentrated in vacuo
  10. customto give a yellow oil
  11. customThe oil was purified by column chromatography on silica gel
  12. washeluting with dichloromethane

出典と根拠

ORDレコード
ord-b546bb7d2476469faddf9cb39b706090
出典データセット
uspto-grants-2009_07
特許番号
US07557121B2

関連ノート

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