Trimethylsilyl triflate → HCID 86690105, 화합물

HRID 520392

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HRID 520392 반응식
[O:1]=[C:2]1[CH2:9][CH:8]2[CH:4]([CH2:5][CH:6]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:7]2)[CH2:3]1.FC(F)(F)S(O[Si](C)(C)C)(=O)=O.C[Si](C)([O:30][CH2:31][CH2:32]O[Si](C)(C)C)C>C(Cl)Cl>[CH2:3]1[CH:4]2[CH:8]([CH2:7][CH:6]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:5]2)[CH2:9][C:2]21[O:30][CH2:31][CH2:32][O:1]2

참가 물질

5

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온도
-78 °C

실험 절차

To a solution of ethyl 5-oxooctahydropentalene-2-carboxylate (210 mg) in DCM (5 mL) cooled to −78° C. were added slowly trimethylsilyl trifluoromethanesulfonate (11.89 mg, 0.054 mmol) and 2,2,7,7-tetramethyl-3,6-dioxa-2,7-disilaoctane (287 mg, 1.391 mmol) under nitrogen. After stirring at −78° C. for 30 min, the reaction mixture was warmed to rt and stirred at rt for 16 h. The reaction was quenched with anhydrous pyridine at −78° C. followed by sat. NaHCO3, and then extracted with EtOAc. The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography to afford ethyl hexahydro-1′H-spiro[[1,3]dioxolane-2,2′-pentalene]-5′-carboxylate (a mixture of endo/exo isomers) as a clear oil.

후처리

  1. temperaturethe reaction mixture was warmed to rt
  2. stirringstirred at rt for 16 h
  3. customThe reaction was quenched with anhydrous pyridine at −78° C.
  4. extractionextracted with EtOAc
  5. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-e79d6d27da3542bbb9b8e6cfad961f63
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09326973B2

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