Propargyl bromide → 5-Hydroxy-7-propargyloxy-2,2-dimethyl-4-chromanone

HRID 1073387Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1073387
C(=O)([O-])[O-].[K+].[K+].[CH2:7](Br)[C:8]#[CH:9].[OH:11][C:12]1[CH:21]=[C:20]([OH:22])[CH:19]=[C:18]2[C:13]=1[C:14](=[O:25])[CH2:15][C:16]([CH3:24])([CH3:23])[O:17]2>CC(CC)=O.[I-].[K+]>[OH:11][C:12]1[CH:21]=[C:20]([O:22][CH2:9][C:8]#[CH:7])[CH:19]=[C:18]2[C:13]=1[C:14](=[O:25])[CH2:15][C:16]([CH3:23])([CH3:24])[O:17]2

Komponenten

6

Edukt 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 8213625,7-Dihydroxy-2,2-dimethylchroman-4-one

Produkt 1

HCID 145929635-Hydroxy-7-propargyloxy-2,2-dimethyl-4-chromanoneAusbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 4875Potassium IodideKatalysatorHCID 6569Methyl Ethyl KetoneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

In 60 ml of methyl-ethyl-ketone 4.2 g of 5,7-dihydroxy-2,2-dimethyl-4-chromanone are dissolved, whereupon 3.0 g (22 millimoles) of potassium carbonate, 0.2 g of potassium iodide, and 3.0 g (2.3 ml, 25 millimoles) of propargyl bromide are added and the reaction mixture is reflexed for 4 hours. The inorganic salt is filtered off, the residue is taken up in 100 ml of carbon tetrachloride and extracted twice with 25 ml of a 5% sodium hydroxide solution each. The aqueous-alkaline layer is cooled to 0° C. The aqueous-alkaline layer is cooled to 0° C. The precipitated sodium phenolate salt is filtered off, washed twice with 20 ml of acetone each, and suspended in 25% hydrochloric acid (50 ml). The mixture is stirred at 5° C. for an hour. The precipitated white product is filtered off, washed twice with 20 ml of water each and dried to constant weight. The crude product thus obtained can be directly subjected to further reactions. Thus 3.7 g of the desired compound are obtained, yield 75% Mp.: 122°-124° C.

Aufarbeitung

  1. additionare added
  2. filtrationThe inorganic salt is filtered off
  3. extractionextracted twice with 25 ml of a 5% sodium hydroxide solution each
  4. temperatureThe aqueous-alkaline layer is cooled to 0° C
  5. filtrationThe precipitated sodium phenolate salt is filtered off
  6. washwashed twice with 20 ml of acetone each, and
  7. filtrationThe precipitated white product is filtered off
  8. washwashed twice with 20 ml of water each and
  9. customdried to constant weight
  10. customThe crude product thus obtained can

Quellen und Nachweise

ORD-Eintrag
ord-56d9670cf8794dc6a526caf07d1572f8
Quelldatensatz
uspto-grants-1990_11
Patentnummer
US04968819

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