Triethylamine → 3-(2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2-one

HRID 132642

Reaktionsgleichung

Reaktionsgleichung von HRID 132642
F[C:2]1[CH:7]=[C:6](F)[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10]C(O)=O.[CH3:14][C:15]([CH3:20])(C)[C:16](Cl)=[O:17].[Li+].[Cl-].C[C@H]1[C@@H](C2C=CC=CC=2)[O:27][C:26](=[O:35])[NH:25]1.[CH2:36](N(CC)CC)[CH3:37]>C1COCC1>[CH3:14][C:15](=[CH:20][CH2:36][CH3:37])[C:16]([N:25]1[CH:9]([C:3]2[CH:2]=[CH:7][CH:6]=[CH:5][CH:4]=2)[CH2:10][O:35][C:26]1=[O:27])=[O:17]

Komponenten

7

Edukt 5

HCID 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 433294Lithium ChlorideHCID 8531614-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 49863953-(2,4-difluorophenyl)propanoic Acid

Produkt 1

HCID 690482483-(2-Methyl-pent-2-enoyl)-4-phenyl-oxazolidin-2-oneAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A flask was charged with 29.5 g (158 mmol) of 3-(2,4-difluoro-phenyl)-propionic acid, 700 mL of THF, and 82.8 mL of triethylamine. The mixture was cooled to 0° C. and 23.4 mL of trimethyl acetyl chloride was added slowly. The mixture was stirred cold for 1 hour. Then 8.06 g (190 mmol) of LiCl and 28.1 g of (4S,5R)-4-methyl-5-phenyl-oxazolidin-2-one was added. The mixture was allowed to warm room temperature and stirred overnight. The solids were filtered off, and the solvent was removed under reduced pressure. The residue was taken up in diethyl ether and washed with sat. aq. ammonium chloride, sat. aq. sodium bicarbonate, and the solvent were removed under reduced pressure. The crude residue was purified by column chromatography (3:1 dichloromethane/hexanes eluent) to give 54 g (99% yield) of the titled compound.

Aufarbeitung

  1. temperatureto warm room temperature
  2. stirringstirred overnight
  3. filtrationThe solids were filtered off
  4. customthe solvent was removed under reduced pressure
  5. washwashed with sat. aq. ammonium chloride, sat. aq. sodium bicarbonate
  6. customthe solvent were removed under reduced pressure
  7. customThe crude residue was purified by column chromatography (3:1 dichloromethane/hexanes eluent)

Quellen und Nachweise

ORD-Eintrag
ord-289944013d874fbd9224757487df27d7
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07388023B2

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