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Methyl 1,4-dioxaspiro[4.5]dec-7-ene-8-carboxylate → 1,4-Dioxaspiro[4.5]dec-7-en-8-ylmethanol

HRID 1741027
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HRID 1741027 반응식
[O:1]1[C:5]2([CH2:10][CH2:9][C:8]([C:11](OC)=[O:12])=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.[H-].C([Al+]CC(C)C)C(C)C>C1COCC1>[O:1]1[C:5]2([CH2:10][CH2:9][C:8]([CH2:11][OH:12])=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 12563052Methyl 1,4-dioxaspiro[4.5]dec-7-ene-8-carboxylateHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 109649381,4-Dioxaspiro[4.5]dec-7-en-8-ylmethanol수율 92.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 1,4-dioxaspiro[4,5]dec-7-ene-8-carboxylate [J. Org. Chem. 40, 538 (1975)] (1.00 g, 5.0 mmol) was stirred under Ar in dry THF (50 ml) at -78° C. as diisobutylaluminium hydride (1.5M in toluene, 8.4 ml, 12.6 mmol) was added dropwise. The mixture was stirred, warming to ambient temperature, for 2.5 h, and then quenched by successive addition of methanol (9 ml), ethanol (9 ml) and water (9 ml). The gelatinous mixture was diluted with ethyl acetate, and filtered through kieselguhr. The filtrate was washed with brine, dried (Na2SO4) and evaporated to give the title compound (0.79 g, 92%) as a colourless oil.

후처리

  1. additionwas added dropwise
  2. customquenched by successive addition of methanol (9 ml), ethanol (9 ml) and water (9 ml)
  3. additionThe gelatinous mixture was diluted with ethyl acetate
  4. filtrationfiltered through kieselguhr
  5. washThe filtrate was washed with brine
  6. dry with materialdried (Na2SO4)
  7. customevaporated

출처 및 근거

ORD 기록
ord-c582ef55e69146c5863d9781f971aeaa
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05972979

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