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1,4-Dioxaspiro[4.5]decan-8-one → 8-Benzyl-1,4-dioxaspiro[4.5]decan-8-ol

HRID 270026
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HRID 270026 반응식
[CH2:1]([Mg]Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:10]1[O:20][C:13]2([CH2:18][CH2:17][C:16](=[O:19])[CH2:15][CH2:14]2)[O:12][CH2:11]1>C1COCC1>[CH2:1]([C:16]1([OH:19])[CH2:17][CH2:18][C:13]2([O:20][CH2:10][CH2:11][O:12]2)[CH2:14][CH2:15]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 5674151,4-Dioxaspiro[4.5]decan-8-oneHCID 178418336HCID 178418336, 화합물

생성물 1

HCID 221798308-Benzyl-1,4-dioxaspiro[4.5]decan-8-ol수율 81%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A 0° C. solution of 2M benzylmagnesium chloride in THF (20 mL) was treated with a solution of 1,4-cyclohexanedione mono-ethylene ketal (6.24 g, 40 mmol) in THF (50 mL), warmed to room temperature, stirred overnight, quenched with saturated NH4Cl (100 mL), and extracted with ethyl acetate (3×100 mL). The combined extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate to provide the desired product (8.08 g, 81%). MS (CI) m/e 231(M−18), 249 (M+H), 266.2 (M+18)+.

후처리

  1. customquenched with saturated NH4Cl (100 mL)
  2. extractionextracted with ethyl acetate (3×100 mL)
  3. washThe combined extracts were washed with water and brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate

출처 및 근거

ORD 기록
ord-a769667b99c14a30ac18f08da6c5c5be
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07449485B2

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