Acetic Acid → 4-(4-(4-Bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-penten-1-ol

HRID 4462

Reaktionsgleichung

[Br:1][C:2]1[CH:25]=[CH:24][C:5]([O:6][C:7]2[CH:23]=[CH:22][C:10]([O:11][CH:12]([CH3:21])[C:13]([O:19][CH3:20])=[CH:14][C:15](OC)=[O:16])=[CH:9][CH:8]=2)=[C:4]([F:26])[CH:3]=1.CC(C[AlH]CC(C)C)C.CCOCC.C(O)(=O)C>C1(C)C=CC=CC=1.O>[Br:1][C:2]1[CH:25]=[CH:24][C:5]([O:6][C:7]2[CH:23]=[CH:22][C:10]([O:11][CH:12]([CH3:21])[C:13]([O:19][CH3:20])=[CH:14][CH2:15][OH:16])=[CH:9][CH:8]=2)=[C:4]([F:26])[CH:3]=1

Komponenten

Reaktionsbedingungen

Temperatur: -78 °C

Versuchsvorschrift

To a solution of 4.5 g (10.6 mmol) 4-(4-(4-bromo-2-fluorophenoxy)phenoxy)-3-methoxy-2-pentenoic acid, methyl ester in 25 ml toluene at -78° C. was added dropwise over a period of 30 min, 16.5 ml of 1.5M DIBAL-H in toluene, keeping the temperature below -60° C. The mixture was stirred for 21/2 hours at -78° C. To the mixture was added 17 ml of a 75:25:6 ether:acetic acid:water mixture, keeping the temperature below -60° C. The mixture was then allowed to warm to room temperature and the solid material was filtered off. The filtrate was washed twice with saturated NaHCO3 and once with water, dried over MgSO4 and the solvent was removed by rotary evaporation. The residue was purified by HPLC, eluting with 80:20 hexane:acetone, to give 3.1 g (74%) of the product as a pale yellow oil which was used immediately in the next reaction.

Aufarbeitung

customthe temperature below -60° C
customthe temperature below -60° C
temperatureto warm to room temperature
filtrationthe solid material was filtered off
washThe filtrate was washed twice with saturated NaHCO3 and once with water
dry with materialdried over MgSO4
customthe solvent was removed by rotary evaporation
customThe residue was purified by HPLC
washeluting with 80:20 hexane

Quellen und Nachweise

ORD-Eintrag: ord-06486a43573049c0972d0737d58446eb
Quelldatensatz: uspto-grants-1988_02
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US04725683

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