Ethyl vinyl ether → 1-Bromo-5-vinyloxy-cyclopentene

HRID 1178359

Reaktionsgleichung

Reaktionsgleichung von HRID 1178359
[Br:1][C:2]1[CH:3]([OH:7])[CH2:4][CH2:5][CH:6]=1.[CH:8](OCC)=[CH2:9]>[Hg](OC(C)=O)OC(C)=O>[Br:1][C:2]1[CH:3]([O:7][CH:8]=[CH2:9])[CH2:4][CH2:5][CH:6]=1

Komponenten

4

Versuchsvorschrift

A solution of 2-bromo-cyclopent-2-enol (Intermediate D3) (21.7 g, 133.1 mmol) in ethyl vinyl ether (300 mL) was treated with Hg(OAc)2 (31.8 g, 99 mmol) at rt for 60 h. The mixture was quenched with 5% NaOH (150 mL) and filtered through celite. The residue was concentrated to yield 1-bromo-5-vinyloxy-cyclopentene as a pale yellow oil, 14.2 g (46%). 1-Bromo-5-vinyloxy-cyclopentene (14.1 g, 74.4 mmol) in toluene was heated in a re-sealable tube at 130° C. for 24 h. (2-Bromo-cyclopent-2-enyl)-acetaldehyde (Intermediate ONE1) was isolated after flash chromatography on silica gel with hexanes to 5% ethyl acetate:hexanes, 10.4 g (74%).

Aufarbeitung

  1. customThe mixture was quenched with 5% NaOH (150 mL)
  2. filtrationfiltered through celite
  3. concentrationThe residue was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-b1d725d08e564ea78de78bd2400582a4
Quelldatensatz
uspto-grants-2007_10
Patentnummer
US07276522B2

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