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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22575Generated: October 25, 2026

Sodium Iodide → 4-Allyloxymandelic acid

https://huagongshe.com/reaction/22575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAllyl bromideHCID 7841—
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Hydroxy-2-(4-hydroxyphenyl)acetic acid, sodium salt hydrateHCID 23698133—
SolventMethanolHCID 887—
Product4-Allyloxymandelic acidHCID 1993056470%
Product4-Methallyloxymandelic acidHCID 19930566—

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428177
Source datasetuspto-grants-1995_06
ORD IDord-c5f188d297c44361a81bdec3606b483a
Source noteuspto-grants-1995_06