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tert-Butyl hydroperoxide → (2R,3R)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2,3-epoxy-2-methylbutanol

HRID 247635
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 247635
C([C@H]([C@@H](C(OCCCC)=O)O)O)(OCCCC)=[O:2].[CH3:19][O:20][C:21]1[C:26]([CH3:27])=[C:25]([CH3:28])[C:24]([O:29][CH3:30])=[C:23]([CH3:31])[C:22]=1[CH2:32][CH:33]=[C:34]([CH3:37])[CH2:35][OH:36].C(OO)(C)(C)C.[OH-].[Na+]>C(Cl)Cl.C(OCC)C.CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-].[Ti+4]>[CH3:19][O:20][C:21]1[C:26]([CH3:27])=[C:25]([CH3:28])[C:24]([O:29][CH3:30])=[C:23]([CH3:31])[C:22]=1[CH2:32][C@H:33]1[O:2][C@:34]1([CH3:37])[CH2:35][OH:36]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 6410tert-Butyl hydroperoxideHCID 14798Sodium Hydroxide2×HCID 6992610Dibutyl D-tartrateHCID 542146164-(2',5'-Dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-2-butenol

Produkt 1

HCID 18602181(2R,3R)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2,3-epoxy-2-methylbutanolAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel

3
HCID 11026Titanium isopropoxideKatalysatorHCID 3283Diethyl EtherLösungsmittelHCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

0.594 ml of titanium tetraisopropoxide was dissolved in 10 ml of dry methylene chloride. Thereupon, 524 mg of dibutyl D-tartrate were added dropwise at -20° C. and the mixture was left to stand at -20° C. for 10 minutes. 197 mg of 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-2-butenol were then added and subsequently a further 180 mg of tert.butyl hydroperoxide (80%) were added dropwise (as a solution in 0.5 ml of methylene chloride). The thus-obtained yellow solution was left to stand at -20° C. for 4 to 5 days, then treated with 5 ml of 1N sodium hydroxide solution, left to warm to room temperature and stirred for 1 hour. The phases were then separated, the aqueous phase was washed twice with methylene chloride, the organic phases were dried over sodium sulphate and concentrated. The colourless oil obtained was dissolved in 20 ml of ethyl ether and stirred with 5 ml of 1N sodium hydroxide solution for 1 hour. The phases were again separated, the aqueous phase was washed twice with ethyl ether, the organic phases were dried over sodium sulphate and concentrated. There were obtained 188 mg (98%) of (2R,3R)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2,3-epoxy-2-methylbutanol.

Aufarbeitung

  1. waitthe mixture was left
  2. waitThe thus-obtained yellow solution was left
  3. waitto stand at -20° C. for 4 to 5 days
  4. waitleft
  5. customThe phases were then separated
  6. washthe aqueous phase was washed twice with methylene chloride
  7. dry with materialthe organic phases were dried over sodium sulphate
  8. concentrationconcentrated
  9. customThe colourless oil obtained
  10. customThe phases were again separated
  11. washthe aqueous phase was washed twice with ethyl ether
  12. dry with materialthe organic phases were dried over sodium sulphate
  13. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-60d80088032f4a68a2aacbc59f880feb
Quelldatensatz
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04709055

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