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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5356Generated: October 28, 2026

Methyl iodide → HCID 19795770, compound

https://huagongshe.com/reaction/5356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-bromo-3-chloro-4-hydroxy-5-methoxybenzaldehydeHCID 262336—
SolventAcetonitrileHCID 6342—
ProductHCID 19795770HCID 1979577071%

Reaction Steps

Into 50 ml of acetonitrile were suspended 5.39 g (20.3 mmol), of 6-bromo-5-chlorovanillin, and 3.04 ml (20.3 mmol) of 1.8-diazabicyclo[5,4,0]-7-undecene and 2.53 ml (40.6 mmol) of methyl iodide were added dropwise under cooling with ice. After stirred for 5 hours at room temperature, 3.9 ml (22.33 mmol) if diisopropylethylamine and 2.53 ml (40.6 mmol) of methyl iodide were added under cooling with ice and the mixture was stirred for 20 hours at room temperature. After distilled off the solvent, 200 ml of dichloromethane were added to the residue, which was washed with water. After dried over anhydrous magnesium sulfate, the concentrated residue was purified by means of silica gel column chromatography (hexane-AcOEt 5:1) to obtain 4.04 g (yield 71%) of title compound as colorless needle-like crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244892
Source datasetuspto-grants-1993_09
ORD IDord-c84f1c46a858498aa1a36a9d1af38093
Source noteuspto-grants-1993_09