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Formaldehyde → tert-Butyl 4-[2-(methylamino)ethyl]piperidine-1-carboxylate

HRID 1480434
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HRID 1480434 반응식
[NH2:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:6][CH2:5]1.C=O.[C:19](O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl.C(O)(=O)C>[CH3:19][NH:1][CH2:2][CH2:3][CH:4]1[CH2:5][CH2:6][N:7]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])[CH2:8][CH2:9]1
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참가 물질

6

반응물 3

HCID 712FormaldehydeHCID 1514258tert-Butyl 4-(2-aminoethyl)piperidine-1-carboxylateHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 46835695tert-Butyl 4-[2-(methylamino)ethyl]piperidine-1-carboxylate

시약·촉매·용매 2

HCID 176Acetic Acid촉매HCID 6344Dichloromethane
용매

실험 절차

Tert-butyl 4-(2-aminoethyl)piperidine-1-carboxylate (1.0 g, 4.38 mmol) was dissolved in DCM (40 ml) and treated with 36.5% formaldehyde solution (326 μl, 4.38 mmol) followed by acetic acid (1 drop). The reaction mixture was stirred for 20 mins and treated with sodium triacetoxyborohydride (93 mg, 0.438 mmol). The resulting mixture was stirred at ambient temperature for 16 hrs and quenched with 2M NaOH (40 ml). The mixture was extracted with DCM (2×100 ml) and the combined organic extracts were dried (MgSO4) and concentrated under reduced pressure to give tert-butyl 4-(2-(methylamino)ethyl)piperidine-1-carboxylate as an oil;

후처리

  1. stirringThe resulting mixture was stirred at ambient temperature for 16 hrs
  2. customquenched with 2M NaOH (40 ml)
  3. extractionThe mixture was extracted with DCM (2×100 ml)
  4. dry with materialthe combined organic extracts were dried (MgSO4)
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e445386113dd44bb933994f9f910d2da
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409895B2

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