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Acetic Acid → (+/-)-1-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}piperazine

HRID 585639
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HRID 585639 반응식
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][O:13][CH3:14])[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:20][CH2:19][CH2:18][C:17](=O)[CH2:16]1.[NH:22]1[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.C[N+](C)(C)C.C(O)(=O)C>ClC(Cl)C>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:10]=[C:9]([O:11][CH2:12][O:13][CH3:14])[CH:8]=[CH:7][C:6]=1[CH:15]1[CH2:20][CH2:19][CH2:18][CH:17]([N:22]2[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)[CH2:16]1
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참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 4837Piperazine2회HCID 13696215Tetramethylammonium Triacetoxyborohydride (>90%)2회HCID 22337753(+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone

생성물 1

HCID 22337793(+/-)-1-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}piperazine

시약·촉매·용매 1

HCID 6365
1,1-Dichloroethane
용매

실험 절차

(±)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone (80 mg) and piperazine (24 mg) were dissolved in dichloroethane (5 ml) and stirred at ambient temperature for 1 hr under argon. Tetramethylammonium triacetoxyborohydride (79 mg) was added and stirring continued under argon. After 16 hr, additional portions of piperazine (24 mg) and tetramethylammonium triacetoxyborohydride (79 mg) were added and stirring continued. After a further 6 hr, glacial acetic acid was added dropwise until a solution was obtained, and stirring continued at ambient temperature. After a further 16 hr, the reaction mixture was partitioned between sodium hydrogen carbonate (20 ml of a saturated solution) and ethyl acetate. The aqueous layer was extracted with ethyl acetate (3×20 ml), and the combined organic extracts were dried over magnesium sulfate and evaporated in vacuo. The crude residue was purified by flash column chromatography chromatography (SiO2, dichloromethane/methanol, 9:1 v/v) to furnish the title compound as an off white solid (52 mg, 53%) and mixture of diastereoisomers; m/z (ES+) 365 (M+H)+.

후처리

  1. stirringstirring
  2. waitAfter 16 hr
  3. stirringstirring
  4. waitAfter a further 6 hr
  5. customwas obtained
  6. stirringstirring
  7. customcontinued at ambient temperature
  8. waitAfter a further 16 hr
  9. customthe reaction mixture was partitioned between sodium hydrogen carbonate (20 ml of a saturated solution) and ethyl acetate
  10. extractionThe aqueous layer was extracted with ethyl acetate (3×20 ml)
  11. dry with materialthe combined organic extracts were dried over magnesium sulfate
  12. customevaporated in vacuo
  13. customThe crude residue was purified by flash column chromatography chromatography (SiO2, dichloromethane/methanol, 9:1 v/v)

출처 및 근거

ORD 기록
ord-8b09e343a70949ef9af2394c6c501c03
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06933319B2

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