Water → 2-(1-Fluoro-4-pentynyl)-4,5-dihydro-4,4-dimethyloxazole

HRID 236030

Reaktionsgleichung

Reaktionsgleichung von HRID 236030
[F:1][CH:2]([CH2:6][CH2:7][C:8]#[CH:9])[C:3]([OH:5])=O.[NH2:10][C:11]([CH3:15])([CH3:14])[CH2:12]O.O>C1(C)C(C)=CC=CC=1>[F:1][CH:2]([C:3]1[O:5][CH2:12][C:11]([CH3:15])([CH3:14])[N:10]=1)[CH2:6][CH2:7][C:8]#[CH:9]

Komponenten

5

Edukt 3

HCID 962WaterHCID 118072-Amino-2-methyl-1-propanolHCID 130449502-Fluorohex-5-ynoic acid

Produkt 1

HCID 130449512-(1-Fluoro-4-pentynyl)-4,5-dihydro-4,4-dimethyloxazoleAusbeute 57 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7237O-XyleneLösungsmittel

Versuchsvorschrift

A mixture of 2-fluoro-5-hexynoic acid (3.0 g, 23.05 mmol) and 2-amino-2-methyl-1-propanol (2.05 g, 23.05 mmol) in 150 ml of dry xylene was refluxed for 16 h. The water formed during the reaction was removed by Linde 3A molecular sieves (15 g) contained in a continuous extractor. The xylene was then distilled off at atmospheric pressure, and the resulting pot material was taken into ether (100 ml). The ethereal solution was washed with saturated sodium bicarbonate solution, water, and dried over MgSO4. Evaporation of ether at 35° C./~35 mm, and distillation of the resulting crude product gave 2.4 g (57%) of 2-(1-fluoro-4-pentynyl)-4,5-dihydro-4,4-dimethyloxazole as a colorless liquid, bp 62°-66° C./0.6 mmHg.

Aufarbeitung

  1. temperaturewas refluxed for 16 h
  2. customwas removed by Linde 3A molecular sieves (15 g)
  3. distillationThe xylene was then distilled off at atmospheric pressure
  4. washThe ethereal solution was washed with saturated sodium bicarbonate solution, water
  5. dry with materialdried over MgSO4
  6. customEvaporation of ether at 35° C./
  7. distillation~35 mm, and distillation of the resulting crude product

Quellen und Nachweise

ORD-Eintrag
ord-3f005f8590e84160881ebbf91e673f74
Quelldatensatz
uspto-grants-1987_02
Patentnummer
US04642364

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