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2-Propen-1-one, 1-(hydroxyphenyl)-3-phenyl- → HCID 11805918, Verbindung

HRID 1462954
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1462954
O[C:2]1[CH:17]=[CH:16][CH:15]=[CH:14][C:3]=1[C:4](=[O:13])[CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[BH4-].[Na+]>C(O)C>[O:13]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]1[C:3]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:2]=1
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Komponenten

4

Edukt 2

HCID 146112-Propen-1-one, 1-(hydroxyphenyl)-3-phenyl-HCID 4311764Sodium borohydride

Produkt 1

HCID 11805918HCID 11805918, VerbindungAusbeute 75,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

2'-Hydroxychalcone (9.0 g) was stirred with ethanol (100 ml) at room temperature whilst sodium borohydride (3.05 g) was added in small portions. After 2 hr. stirring the colourless solution was evaporated to dryness and acetic acid (100 ml) added. Toluene sulphonic acid (1.0 g) was added and the solution was heated on the steam bath for 30 min. The solution was diluted with water and extracted with toluene. The extract was washed with saturated sodium bicarbonate solution, dried over magnesium sulphate, and evaporated. The residue was chromatographed on neutral alumina to yield flav-3-ene (6.3 g) as an oil, identified by its n.m.r. spectrum. The multiplet at 5.8 p.p.m. is characteristic of flav-3-enes.

Aufarbeitung

  1. additionwas added in small portions
  2. customwas evaporated to dryness and acetic acid (100 ml)
  3. additionadded
  4. additionToluene sulphonic acid (1.0 g) was added
  5. temperaturethe solution was heated on the steam bath for 30 min
  6. additionThe solution was diluted with water
  7. extractionextracted with toluene
  8. washThe extract was washed with saturated sodium bicarbonate solution
  9. dry with materialdried over magnesium sulphate
  10. customevaporated
  11. customThe residue was chromatographed on neutral alumina

Quellen und Nachweise

ORD-Eintrag
ord-fa1ffa66b37f42fea7f801760edf3c61
Quelldatensatz
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04461907

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