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Cyclohexene oxide → rel-(1R,2R)-2-(1-Pyrrolidinyl)cyclohexanol

HRID 589419
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HRID 589419 반응식
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:6]12[O:12][CH:7]1[CH2:8][CH2:9][CH2:10][CH2:11]2>O>[N:1]1([C@@H:6]2[CH2:11][CH2:10][CH2:9][CH2:8][C@H:7]2[OH:12])[CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 9246Cyclohexene oxideHCID 31268Pyrrolidine

생성물 1

HCID 10103566rel-(1R,2R)-2-(1-Pyrrolidinyl)cyclohexanol수율 98%

시약·촉매·용매 1

HCID 962Water용매

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온도
90 °C

실험 절차

Pyrrolidine (4.26 g, 60 mmol) was added to a solution of cyclohexene oxide (1.96 g, 20 mmol) in H2O (6 mL), and the resulting mixture was heated at 90° C. for 16 hours. After cooling, the solvent was removed under reduced pressure and the resulting residue was extracted with DCM (10 mL×3). The organic phasew were combined and dried with anhydrous Na2SO4. After removing the Na2SO4 by filtration, the solvent was evaporated and the material dried under vacuum to afford the desired compound (+/−)-1 (3.3 g, 19.5 mmol, yield 98%). 1H NMR (CDCl3) δ 4.06 (s, 1H), 3.45-3.30 (m, 1H), 2.75-2.63 (m, 2H), 2.62-2.50 (m, 2H), 2.51-2.42 (m, 1H), 1.90-1.58 (m, 8H), 1.45-1.15 (m, 4H).

후처리

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure
  3. extractionthe resulting residue was extracted with DCM (10 mL×3)
  4. dry with materialdried with anhydrous Na2SO4
  5. customAfter removing the Na2SO4
  6. filtrationby filtration
  7. customthe solvent was evaporated
  8. customthe material dried under vacuum

출처 및 근거

ORD 기록
ord-c2c926ca4e4d45af9dfb774d48d92523
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09233168B2

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