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Water → 5-Bromo-2-(1,4-dioxaspiro[4,5]decane-8-yl)pyridine

HRID 1748521
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1748521
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2(C(O)=O)[CH2:17][CH2:16][C:11]3([O:15][CH2:14][CH2:13][O:12]3)[CH2:10][CH2:9]2)=[N:6][CH:7]=1.O>CS(C)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:17][CH2:16][C:11]3([O:15][CH2:14][CH2:13][O:12]3)[CH2:10][CH2:9]2)=[N:6][CH:7]=1
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Komponenten

4

Edukt 2

HCID 962WaterHCID 86692469HCID 86692469, Verbindung

Produkt 1

HCID 866924705-Bromo-2-(1,4-dioxaspiro[4,5]decane-8-yl)pyridineAusbeute 95,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 679Dimethyl SulfoxideLösungsmittel

Versuchsvorschrift

A solution of 8-(5-bromopyridin-2-yl)-1,4-dioxaspiro[4,5]decane-8-carboxylic acid (776 mg) in dimethylsulfoxide (3 ml) was stirred at 150° C. for 1.5 hours. After completion of the reaction, the reaction solution was left stand to room temperature, water was added and extracted with ethyl acetate. The organic solution was washed with water and saturated brine successively, dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give 5-bromo-2-(1,4-dioxaspiro[4,5]decane-8-yl)pyridine (646 mg) as a colorless oil.

Aufarbeitung

  1. customAfter completion of the reaction
  2. waitthe reaction solution was left stand to room temperature
  3. extractionextracted with ethyl acetate
  4. washThe organic solution was washed with water and saturated brine successively
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated
  7. customThe resulting residue was purified with silica gel column chromatography (n-hexane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-5118ec4367134c6eb7f59ac36ad38b3a
Quelldatensatz
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09150555B2

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