Acrolein → (2R)-Bicyclo[2.2.2]oct-5-ene-2-carboxaldehyde

HRID 381704노트

반응식

HRID 381704 반응식
Cl.[CH2:2]([C@@H:9]1NC(C)(C)N(C)[C:10]1=[O:17])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(C=C)=O.C1CCC=CC=1>CC#N.O.CCOCC>[CH:6]12[CH2:5][CH2:4][CH:3]([CH:8]=[CH:7]1)[CH2:2][C@H:9]2[CH:10]=[O:17]

참가 물질

6

실험 절차

To a solution of 5 (32 mg, 0.12 mmol) in CH3CN/H2O (95/5 v/v, 1.0 M) was added acrolein (501 μL, 7.5 mmol), and cyclohexadiene (238 μL, 2.5 mmol). The solution was stirred for 24 h, after which time the reaction mixture was diluted with Et2O (10 mL) and washed with H2O (10 mL). The aqueous layer was extracted with Et2O (10 mL×2) and the combined organics were dried (Na2SO4), and concentrated. Purification by silica gel chromatography (10% ether/pentane) afforded the title compound as a colorless oil in 82% yield (280 mg, 2.06 mmol); 14:1 endo:exo; 94% ee. Product ratios were determined by GLC (Bodman Γ-TA column, 75° C. isotherm, 23 psi) tr=51.0 min and 54.4 min. 1H NMR, 13C NMR, and IR data were consistent with previously reported values (Ishihara et al. (1998), supra).

후처리

  1. washwashed with H2O (10 mL)
  2. extractionThe aqueous layer was extracted with Et2O (10 mL×2)
  3. dry with materialthe combined organics were dried (Na2SO4)
  4. concentrationconcentrated
  5. customPurification by silica gel chromatography (10% ether/pentane)

출처 및 근거

ORD 기록
ord-9aa4addca11c4ecc9de0cc57d96954b5
출처 데이터셋
uspto-grants-2001_10
특허 번호
US06307057B1

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