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

HRID 1846413
ノート
印刷プレビュー

反応式

HRID 1846413 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 9246Cyclohexene oxideHCID 31268Pyrrolidine

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
90 °C

実験手順

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 phases 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).

後処理

  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

出典と根拠

ORDレコード
ord-b50f77da268245bcb28d70fd7e4ac310
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08952032B2

反応ノート

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