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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22575Erstellt: 23. Oktober 2026

Sodium Iodide → 4-Allyloxymandelic acid

https://huagongshe.com/de/reaction/22575

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktAllyl bromideHCID 7841—
Edukt3-Chloro-2-methyl-1-propeneHCID 11241—
EduktPotassium HydroxideHCID 14797—
Edukt2-Hydroxy-2-(4-hydroxyphenyl)acetic acid, sodium salt hydrateHCID 23698133—
LösungsmittelMethanolHCID 887—
Produkt4-Allyloxymandelic acidHCID 1993056470%
Produkt4-Methallyloxymandelic acidHCID 19930566—

Reaktionsschritte

20.8 g (0.10 mol) of 4-hydroxymandelic acid sodium salt monohydrate and 6.6 g (0.10 mol) of potassium hydroxide are dissolved with 1.0 g (6.7 mmol) of sodium iodide in 75 ml of methanol. Then 0.12 mol of allyl bromide (methallyl chloride in the case of methallyl) is added and the reaction mixture is refluxed for 16 hours under nitrogen. The reaction mixture is concentrated on a vacuum rotary evaporator and the residue is acidified with concentrated hydrochloric acid. The product is extracted 3 times with butyl acetate. The organic phases are washed with water, combined, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. Crystallisation of the residue from toluene/petroleum ether give 4-allyloxymandelic acids such as 4-allyloxymandelic acid as an amorphous powder (70%) and 4-methallyloxymandelic acid, m.p. 121°-126° (65%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428177
Quelldatensatzuspto-grants-1995_06
ORD IDord-c5f188d297c44361a81bdec3606b483a
Quellennotizuspto-grants-1995_06