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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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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1741027
[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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Komponenten

4

Edukt 2

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

Produkt 1

HCID 109649381,4-Dioxaspiro[4.5]dec-7-en-8-ylmethanolAusbeute 92,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-c582ef55e69146c5863d9781f971aeaa
Quelldatensatz
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05972979

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