Реакция #977

ord-2a5760aaa3d049789dc0038907f707bb

Уравнение реакции

CCN(CC)CC
triethylamine
C/C(=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1)CO
alcohol
C/C(=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1)CO
(E)-3-[trans-(4-tert-Butyldimethysilyloxycyclohexyl)]-2-methylprop-2-en-1-ol
O=C(Cl)C(=O)Cl
oxalyl chloride
CS(C)=O
dimethylsulfoxide
C/C(C=O)=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1
aldehyde
C/C(C=O)=C\[C@H]1CC[C@H](O[Si](C)(C)C(C)(C)C)CC1
(E)-3-[trans-(4-tert-Butyldimethylsilyloxycyclohexyl)]-2-methylprop-2-en-1-al

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    ДругоеThe reaction was quenched with 1.0N HCl
  3. 3
    Экстракцияthe aqueous layer was extracted with three portions of methylene chloride
  4. 4
    СушкаThe combined organic extracts were dried over MgSO4
  5. 5
    Другоеevaporated to dryness

Методика

To a -78° C. solution of oxalyl chloride (105 μL, 1.2 mmol) in 1.0 mL of methylene chloride was added dimethylsulfoxide (170 μL, 2.4 mmol). The resulting solution was stirred for 5 min and then 170 mg (0.6 mmol) of the alcohol 135 was added in 1.0 mL of methylene chloride. The reaction mixture was stirred at -78° C. for 45 min at which time 500 μL (3.6 mmol) of triethylamine was added and the solution was allowed to warm to ambient temperature. The reaction was quenched with 1.0N HCl and the aqueous layer was extracted with three portions of methylene chloride. The combined organic extracts were dried over MgSO4 and evaporated to dryness to give the crude aldehyde 136 which was used directly in the next reaction. 1H NMR consistent with structure.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05723459uspto-grants-1998_03