HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722004Generated: October 30, 2026
Methyl iodide → 3-Chloro-4-methoxybenzonitrile
https://huagongshe.com/reaction/1722004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzonitrile, 3-chloro-4-hydroxy- | HCID 2735739 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-4-methoxybenzonitrile | HCID 4323105 | — |
Reaction Steps
Under N2, a solution of 3-chloro-4-hydroxybenzonitrile (15.4 g, 0.1 mole) in dry DMF (75 ml) was added rapidly dropwise to a stirred suspension of sodium hydride (4.0 g, 0.1 mole, 60% oil dispersion) in dry DMF (25 ml). After heating at 70° C. for 2 hours, the mixture was cooled to 20° C. and a solution of methyliodide (30 ml) in dry DMF (50 ml) was added dropwise. Following an 18 hour period at room temperature, the precipitate of sodium iodide was removed by filtration and the solvent was stripped from the filtrate under reduced pressure. The crystalline residue was slurried in water and the product was collected to yield 16.8 g (quant.) of 26, m.p. 105°-108° C. A sample recrystallized from IPA-H2O melted at 107°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853383 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-2ca80727694d46209dfa5cb8e5552917 |
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| Source note | uspto-grants-1989_08 |
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