Diethyl Ether → HCID 14838645, Verbindung

HRID 893711Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 893711
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:13][CH:14]=C)[C:5]([OH:12])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].CC[O:18]CC.I([O-])(=O)(=O)=O.[Na+]>[Os](=O)(=O)(=O)=O.O>[C:7]([C:6]1[C:5]([OH:12])=[C:4]([CH2:13][CH:14]=[O:18])[CH:3]=[C:2]([Cl:1])[CH:11]=1)([O:9][CH3:10])=[O:8]

Komponenten

6

Versuchsvorschrift

Osmium tetroxide (1.0 g, 3.9 mmol) was added to a mixture of methyl 5-chloro-2-hydroxy-3-(2-propenyl)benzoate (4c) (22.7 g, 0.1 mol), ether (400 ml), and water (400 ml). After stirring at room temperature for 5 minutes, sodium periodate (47.06 g, 0.22 mol) was added in portions. The mixture was stirred at room temperature for another 21 hours, and then poured into 800 ml of water. The layers were separated and the aqueous layer extracted with ethyl ether (2×400 ml). The organic layers were combined, dried over anhydrous Na2SO4 and then filtered through a column of Florisil (85 g) to remove inorganic impurity Evaporation of the ether yielded 5c quantitatively as a brown solid, m.p. 49° 59° C., which appeared hygroscopic. The crude product was used for the next reaction without purification. NMR (CDCl3) δ 10.90 (s, 1H, OH), 9.67 (t, 1H, J=1.5 Hz, CHO), 7.70 (d, 1H, J=3 Hz, aromatic proton), 7.23 (d, 1H, aromatic proton), 3.97 (s, 3H, CH3) and 3.70(d, 2H, CH2).

Aufarbeitung

  1. stirringThe mixture was stirred at room temperature for another 21 hours
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted with ethyl ether (2×400 ml)
  4. dry with materialdried over anhydrous Na2SO4
  5. filtrationfiltered through a column of Florisil (85 g)
  6. customto remove inorganic
  7. customimpurity Evaporation of the ether

Quellen und Nachweise

ORD-Eintrag
ord-8fb2224b07e44598a3b719b460e310a0
Quelldatensatz
uspto-grants-1992_06
Patentnummer
US05126364

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