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Toluene → 1-methoxy-2-oxabicyclo[3.3.0]octane

HRID 2113244
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HRID 2113244 반응식
[C:1]1(C)C=CC=CC=1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.C([O:28][CH2:29][CH2:30][CH:31]1[CH2:35][CH2:34][CH2:33][C:32]1=[O:36])(=O)C>CO>[CH3:1][O:36][C:32]12[CH2:33][CH2:34][CH2:35][CH:31]1[CH2:30][CH2:29][O:28]2
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 11116481HCID 11116481, 화합물

생성물 1

HCID 103517951-methoxy-2-oxabicyclo[3.3.0]octane수율 95%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A reaction vessel was charged with 21 parts of anhydrous toluene, 0.6 parts of methanol, 0.2 part of pyridinium paratoluene sulfonate (PPTS), 2.0 parts of 2-(2-acetoxyethyl)cyclopentanone (8) obtained in Preparation Example 1 at room temperature. The mixture was refluxed for seven hours with stirring. After the reaction, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane: ethyl acetate=19:1) to obtain 1.6 parts of 1-methoxy-2-oxabicyclo[3.3.0]octane (9) (yield: 95%).

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후처리

  1. customobtained in Preparation Example 1 at room temperature
  2. temperatureThe mixture was refluxed for seven hours
  3. customAfter the reaction
  4. filtrationthe reaction mixture was filtered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe resulting residue was purified by silica gel column chromatography (n-hexane: ethyl acetate=19:1)

출처 및 근거

ORD 기록
ord-dee7a8fcf4544cc6b84b1b90e4fb64f7
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07524978B2

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