Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1460252Erstellt: 25. Oktober 2026

1-Bromo-3-chloropropane → 4-(3-Chloropropoxy)-3-methoxymandelic acid phenylmethyl ester

https://huagongshe.com/reaction/1460252

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-3-chloropropaneHCID 8006—
EduktPotassium CarbonateHCID 11430—
EduktMandelate ionHCID 3839223—
Edukt4-Hydroxy-3-methoxymandelic acid (phenylmethyl) esterHCID 15020367—
LösungsmittelAcetoneHCID 180—
Produkt4-(3-Chloropropoxy)-3-methoxymandelic acid phenylmethyl esterHCID 1502036822%

Reaktionsschritte

A mixture of 2.92 g (0.008 mole) of 4-hydroxy-3-methoxymandelic acid (phenylmethyl) ester, 2 ml (0.02 mole) of 1-bromo-3-chloropropane, and 2.80 g (0.02 mole) of potassium carbonate in 40 ml of acetone was heated at reflux for 16 hours under nitrogen atmosphere during which time the solution changed from colorless to light-yellow. TLC (silica gel, hexanes/acetone 4:1) showed that the mandelate derivative had reacted, but 30-40% of unknown impurities had formed. The inorganic materials were separated by filtration, washed with acetone, and the filtrate was concentrated in vacuo at 60° C. to give 3.65 g of crude product. The material was purified by column chromatography (diameter 25 mm, using 80 g of silica gel) eluted with cyclohexane/ethyl acetate (6:1). The fractions containing the product were collected and the solid recrystallized from ethyl ether/hexanes to give 0.637 g (22%) of material as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05070087
Quelldatensatzuspto-grants-1991_12
ORD IDord-4d7b3694ce944ed48f67ec310306c3a9
Quellennotizuspto-grants-1991_12