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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917980Generated: November 1, 2026

Potassium Iodide → 5-[(3-Phenylprop-2-en-1-yl)oxy]-2H-1,3-benzodioxole

https://huagongshe.com/reaction/917980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantSesamolHCID 68289—
ReactantBenzene, (3-chloro-1-propenyl)-HCID 94242—
SolventAcetoneHCID 180—
Product5-[(3-Phenylprop-2-en-1-yl)oxy]-2H-1,3-benzodioxoleHCID 54275545—

Reaction Steps

A mixture of sesamol (27.6 g.), cinnamyl chloride (30.4 g.), anhydrous potassium carbonate (50.0 g.), potassium iodide (2.0 g.) in anhydrous acetone (100 ml.) was heated under reflux for 1.5 hrs. The acetone was removed by evaporation, and the residue was treated with excess water and cooled to give an oil, which subsequently solidified. The crude product was collected by filtration and recrystallized from methanol to give MDCB as colorless prisms, m.p. 83° C., yield 15.0 g. (Found: C, 75.4; H, 5.67. Calculated for C16H14O3 : C, 75.6; H, 5.55.) The nuclear magnetic resonance (NMR) spectrum of MDCB at 100 MHz in deuterated chloroform (CDCl3) exhibited absorbances as follows: a doublet (2 protons) at δ 4.59 (coupling constant J = 6.0 Hz), a singlet (2 protons) at δ 5.89 a multiplet (5 protons) at δ 6.22-6.80, and a multiplet (5 protons) at δ 7.18-7.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03968234
Source datasetuspto-grants-1976_07
ORD IDord-4b0b3cf1c62740a580a68fbeadf125c5
Source noteuspto-grants-1976_07