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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 704552Erstellt: 25. Oktober 2026

Benzyl Bromide → 6-Benzyloxy-1-hexanol

https://huagongshe.com/reaction/704552

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktHexanediolHCID 147023—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Benzyloxy-1-hexanolHCID 278476372,1%

Reaktionsschritte

Pure potassium t-butoxide (50 mmoles, 5.61 g) is added portionwise to a stirred solution of 100 mmoles of hexanediol (11.82 gr) dissolved in 30 ml of THF at room temperature under argon. When addition is complete, 50 mmoles of benzylbromide (5.9 ml) are introduced and the reaction mixture is stirred at room temperature overnight. The white solid is then removed by filtration, the filtrate is evaporated and the residue is dissolved in ethylacetate, washed with saturated ammonium chloride, H2O and brine. Usual workup and purification by flash chromatography gives finally 7.51 g of product (72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04988680
Quelldatensatzuspto-grants-1991_01
ORD IDord-77dcd2851cee4ee88a5b0d3fe48a05a8
Quellennotizuspto-grants-1991_01