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2-t-Butyl-5-[(E)-2-ethoxycarbonylethenyl]-1-nitrobenzene → 2-t-Butyl-5-[(1E)-3-hydroxy-1-propenyl]-1-nitrobenzene

HRID 1418182
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1418182
[C:1]([C:5]1[CH:10]=[CH:9][C:8](/[CH:11]=[CH:12]/[C:13](OCC)=[O:14])=[CH:7][C:6]=1[N+:18]([O-:20])=[O:19])([CH3:4])([CH3:3])[CH3:2].[H-].C([Al+]CC(C)C)C(C)C>O1CCCC1>[C:1]([C:5]1[CH:10]=[CH:9][C:8](/[CH:11]=[CH:12]/[CH2:13][OH:14])=[CH:7][C:6]=1[N+:18]([O-:20])=[O:19])([CH3:4])([CH3:2])[CH3:3]
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Komponenten

4

Edukt 2

HCID 193484662-t-Butyl-5-[(E)-2-ethoxycarbonylethenyl]-1-nitrobenzeneHCID 21225700Diisobutylaluminumhydride

Produkt 1

HCID 193484672-t-Butyl-5-[(1E)-3-hydroxy-1-propenyl]-1-nitrobenzeneAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

A solution of 9.24 g (33.4 mmol) of 2-t-butyl-5-[(E)-2-ethoxycarbonyl-ethenyl]-1-nitrobenzene [prepared as described in step (ii) above] in 200 ml of tetrahydrofuran was cooled to -70° C. in a dry ice-acetone bath, and 100 ml (100 mmol) of a 1M solution of diisobutylaluminum hydride in tetrahydrofuran were added dropwise thereto over a period of 45 minutes. The resulting mixture was then stirred for a further 30 minutes. At the end of this time, the reaction temperature was allowed to rise to 0° C., and the reaction was quenched by adding dropwise a mixture of 4 ml of methanol and 20 ml of tetrahydrofuran. The reaction mixture was then poured into 2N aqueous hydrochloric acid-ice, after which it was extracted with ethyl acetate. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through 300 g of silica gel, using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 7.06 g (yield 90%) of the title compound as an oily substance.

Aufarbeitung

  1. customto rise to 0° C.
  2. customthe reaction was quenched
  3. additionby adding dropwise
  4. additiona mixture of 4 ml of methanol and 20 ml of tetrahydrofuran
  5. additionThe reaction mixture was then poured into 2N aqueous hydrochloric acid-ice
  6. extractionafter which it was extracted with ethyl acetate
  7. washThe extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order
  8. dry with materialafter which it was dried over anhydrous sodium sulfate
  9. customThe solvent was removed by distillation under reduced pressure
  10. customthe resulting residue was purified by column chromatography through 300 g of silica gel
  11. additionby volume mixture of hexane and ethyl acetate as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-e9b4949aa5694fe0a25cf969cd720c81
Quelldatensatz
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05880147

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