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Ethyl levulinate → Methyl 5-bromo-4-oxopentanoate

HRID 335109
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 335109
[Br:1]Br.[O:3]=[C:4]([CH3:12])[CH2:5][CH2:6][C:7]([O:9][CH2:10]C)=[O:8]>CO>[Br:1][CH2:12][C:4](=[O:3])[CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 10883Ethyl levulinateHCID 24408Bromine

Produkt 1

HCID 9855825Methyl 5-bromo-4-oxopentanoateAusbeute 29,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel2×

Versuchsvorschrift

A solution of bromine (27.71 g, 173.4 mmol) in methanol (40 mL) was added dropwise to a solution of ethyl 4-oxopentanoate (25.0 g, 173.4 mmol) in methanol (200 mL) at room temperature over a period of 30 minute, and the reaction mixture was stirred overnight. The reaction mixture was concentrated, and the residue was partitioned between 3:1 ether:ethyl acetate and water, washed with saturated sodium bicarbonate, water, brine, dried, and concentrated to afford 17 g of a crude clear oil. The oil was purified by MPLC (Biotage) eluting with 8:1 hexane ethyl acetate to afford methyl 5-bromo-4-oxopentanoate (10.65 g, 29.38% yield) as a clear oil. 1H NMR (CDCl3) δ 3.96 (s, 2H), 3.69 (s, 3H), 2.96 (t, 2H), 2.66 (t, 2H).

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated
  2. customthe residue was partitioned between 3:1 ether
  3. washethyl acetate and water, washed with saturated sodium bicarbonate, water, brine
  4. customdried
  5. concentrationconcentrated
  6. customto afford 17 g of a crude clear oil
  7. customThe oil was purified by MPLC (Biotage)
  8. washeluting with 8:1 hexane ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-beb3663988b546f082190100aad21462
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08883828B2

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