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Ethyl Acetate → 8-(3-Methylbutylidene)-1,4-dioxaspiro[4.5]decane

HRID 2249662
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HRID 2249662 반응식
[I-].[CH2:2]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:3][CH:4]([CH3:6])[CH3:5].C([Li])CCC.[O:31]1[C:35]2([CH2:40][CH2:39][C:38](=O)[CH2:37][CH2:36]2)[O:34][CH2:33][CH2:32]1.C(OCC)(=O)C>O1CCCC1.CCCCCC.O>[CH3:5][CH:4]([CH3:6])[CH2:3][CH:2]=[C:38]1[CH2:39][CH2:40][C:35]2([O:34][CH2:33][CH2:32][O:31]2)[CH2:36][CH2:37]1
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참가 물질

8

반응물 4

HCID 8857Ethyl AcetateHCID 5674151,4-Dioxaspiro[4.5]decan-8-oneHCID 22245250(3-Methylbutyl)(triphenyl)phosphanium iodideHCID 178418339Butyllithium

생성물 1

HCID 689871908-(3-Methylbutylidene)-1,4-dioxaspiro[4.5]decane수율 78%

시약·촉매·용매 3

HCID 962
Water
용매
HCID 8028Tetrahydrofuran용매2회
HCID 8058Hexane용매

실험 절차

In 100 ml of tetrahydrofuran is suspended 39.8 g of isopentyltriphenylphosphonium iodide. At −25° C. to −20° C., 52 ml of a 1.6 mol/L solution of n-butyllithium in n-hexane is dropwise added to the suspension. After stirring the mixture thus obtained at −25° C. to −15° C. for one hour, the temperature is elevated to ambient temperature over a period of one hour. A solution of 10.0 g of 1,4-dioxaspiro[4.5]-decan-8-one in 50 ml of tetrahydrofuran is added to the reaction mixture and stirred at ambient temperature for one hour. The reaction mixture is added to a mixture of ethyl acetate and water, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=95:5) to obtain 10.5 g of 8-(3-methylbutylidene)-1,4-dioxaspiro[4.5]decane as a colorless oily product.

후처리

  1. customthus obtained at −25° C. to −15° C. for one hour
  2. stirringstirred at ambient temperature for one hour
  3. customthe organic layer is separated
  4. customThe organic layer thus obtained
  5. washis washed with water and saturated aqueous solution of sodium chloride successively
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationthe solvent is distilled off under reduced pressure
  8. customThe residue thus obtained
  9. customis purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=95:5)

출처 및 근거

ORD 기록
ord-1c69f187b66b4b009de285e49dcb8351
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07314888B1

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