HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5356Generated: October 28, 2026
Methyl iodide → HCID 19795770, compound
https://huagongshe.com/reaction/5356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-bromo-3-chloro-4-hydroxy-5-methoxybenzaldehyde | HCID 262336 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19795770 | HCID 19795770 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244892 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-c84f1c46a858498aa1a36a9d1af38093 |
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| Source note | uspto-grants-1993_09 |
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