Hydrochloric Acid → 4-n-Butyl-1-[4-(2-hydroxyphenyl)-4-oxo-1-butyl]piperidine

HRID 1723890노트

반응식

HRID 1723890 반응식
[CH2:1]([CH:5]1[CH2:10][CH2:9][N:8]([CH2:11][CH2:12][CH2:13][C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[O:22]CC2C=CC=CC=2)=[O:15])[CH2:7][CH2:6]1)[CH2:2][CH2:3][CH3:4].Cl.[OH-].[Na+].C(Cl)Cl.CO>CCO.[Pd]>[CH2:1]([CH:5]1[CH2:6][CH2:7][N:8]([CH2:11][CH2:12][CH2:13][C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[OH:22])=[O:15])[CH2:9][CH2:10]1)[CH2:2][CH2:3][CH3:4]

참가 물질

7

실험 절차

4-n-Butyl-1-[4-(2-hydroxyphenyl)-4-oxol-butyl]piperidine (27)-3 To a 25 mL reaction flask was added a solution of 4-n-Butyl-1-[4-(2-benzyloxyphenyl)-4-oxo-1-butyl]piperidine (26) (49 mg, 1.2 mmol) dissolved in dry EtOH (10 mL) and conc. HCl (0.1 mL) followed by addition of palladium on charcoal (40 mg). The reaction flask was then charged with H2 by the use of balloon technique and left stirring at rt over-night under H2 atmosphere. The reaction mixture was basified by addition of NaOH (2 mL, 2.0 M) and filtered through celite. The aqueous phase was extracted with ethyl acetate (3×50 mL) and the combined organic phases were washed with brine (10 mL) and NaOH (10 mL, 2 M), dried (MgSO4) and evaporated to dryness to produce 0.42 g of crude 27. The crude product was subjected to CC [eluent: : CH2Cl2: MeOH (99:1)] to give pure 27 (0.21 g, 58%); LC-MS [M+H]+ 303 (cald. 303.2).

후처리

  1. additionThe reaction flask was then charged with H2 by the use of balloon technique
  2. waitleft
  3. filtrationfiltered through celite
  4. extractionThe aqueous phase was extracted with ethyl acetate (3×50 mL)
  5. washthe combined organic phases were washed with brine (10 mL) and NaOH (10 mL, 2 M)
  6. dry with materialdried (MgSO4)
  7. customevaporated to dryness
  8. customto produce 0.42 g of crude 27

출처 및 근거

ORD 기록
ord-d3faa60d54944562a28a281ffaaf6aa1
출처 데이터셋
uspto-grants-2009_02
특허 번호
US07485651B2

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