Benzophenone → 1,1-Diphenyl-5-methoxy-1-pentanol

HRID 851301

Reaktionsgleichung

Reaktionsgleichung von HRID 851301
[Mg].Br[CH2:3][CH2:4][CH2:5][CH2:6][O:7][CH3:8].[C:9]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>CCOCC>[C:17]1([C:9]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)([OH:16])[CH2:3][CH2:4][CH2:5][CH2:6][O:7][CH3:8])[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Komponenten

5

Edukt 3

HCID 3102BenzophenoneHCID 5211681-Bromo-4-methoxybutaneHCID 5462224Magnesium

Produkt 1

HCID 131250861,1-Diphenyl-5-methoxy-1-pentanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel3×

Versuchsvorschrift

To a suspension of 3.9 g. (0.16 mole) of magnesium turnings in 300 ml. of dry ether was added dropwise 26.7 g. (0.16 mole) of 1-bromo-4-methoxybutane in 80 ml. of ether and the mixture refluxed for four hours. The reaction mixture was cooled and 14.6 g. (0.008 mole) of benzophenone in 100 ml. of dry ether was added dropwise. The mixture was stirred at ambient temperature for 18 hours, cautiously quenched with water and the ether layer separated. The aqueous layer was extracted with ether and the combined ether extract was dried and concentrated to give 1,1-diphenyl-5-methoxy-1-pentanol, m.p. 112°-115° C.

Aufarbeitung

  1. additionTo a suspension of 3.9 g
  2. temperatureThe reaction mixture was cooled
  3. customcautiously quenched with water
  4. customthe ether layer separated
  5. extractionThe aqueous layer was extracted with ether
  6. extractionthe combined ether extract
  7. customwas dried
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-f96ea3d11f8141bb8c275c39b317d715
Quelldatensatz
uspto-grants-1983_05
Patentnummer
US04383999

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