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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393262Generated: October 29, 2026

Methyl iodide → Isovanillin

https://huagongshe.com/reaction/393262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantLithium CarbonateHCID 11125—
SolventDimethylformamideHCID 6228—
ProductIsovanillinHCID 1212782.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

3,4-Dihydroxybenzaldehyde (2.76 g, 20 mmol) was dissolved in DMF (15 ml), and methyl iodide (37.4 ml, 60 mmol) and anhydrous lithium carbonate (4.4 g, 60 mmol) were successively added to this solution. After being stirred at an external temperature of 90° C. for 1.5 hours, the reaction mixture was cooled to room temperature and the inorganic salt was filtered off. A saturated aqueous solution of ammonium chloride (200 ml) was added to the filtrate to adjust the aqueous layer to a pH of from 7 to 8, and the solution was extracted with ethyl acetate (300 ml×2). The combined organic layer was washed with a saturated aqueous solution of sodium chloride (300 ml), dried over anhydrous magnesium sulfate, filtered to remove the desiccating agent, and concentrated under reduced pressure to give the title compound (2.5 g, 82.2%) (Table 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806276B2
Source datasetuspto-grants-2004_10
ORD IDord-8d389578eefe499790ef594c86dfd171
Source noteuspto-grants-2004_10