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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 743378Erstellt: 24. Oktober 2026

Salicyl Alcohol → Benzenemethanol, 2-(phenylmethoxy)-

https://huagongshe.com/de/reaction/743378

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicyl AlcoholHCID 5146—
EduktBenzyl BromideHCID 7498—
EduktHexaneHCID 8058—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzenemethanol, 2-(phenylmethoxy)-HCID 1881187%

Reaktionsschritte

151 g of potassium t-butoxide were added, whilst ice-cooling and stirring, to a solution of 152 g of salicyl alcohol in 600 ml of dimethylformamide, and the resulting mixture was stirred at room temperature for 30 minutes; 160 ml of benzyl bromide were then added dropwise to the mixture. The reaction mixture was then stirred at a temperature of from 30° to 40° C. for 2 hours, after which it was partitioned between ethyl acetate and water. The organic layer was washed twice, each time with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated by evaporation under reduced pressure. The oily residue thus obtained was subjected to column chromatography through silica gel, using a 5:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 228.5 g (yield 87%) of 2-benzyloxybenzyl alcohol as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05556864
Quelldatensatzuspto-grants-1996_09
ORD IDord-ca8ed899893e4c4988b0ee3b61efe071
Quellennotizuspto-grants-1996_09