HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167333Generated: October 27, 2026
Methyl iodide → 2,4-Dimethoxy-5-methoxymethyl-benzonitrile
https://huagongshe.com/reaction/1167333
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Hydroxymethyl-2,4-dimethoxy-benzonitrile | HCID 22996245 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Dimethoxy-5-methoxymethyl-benzonitrile | HCID 22996188 | 95% |
Reaction Steps
To a solution of 5-hydroxymethyl-2,4-dimethoxy-benzonitrile (218 mg, 1.128 mmol) in tetrahydrofuran (10 mL) cooled to 0° C. were sequentially added sodium hydride (34.2 mg, 1.354 mmol) and iodomethane (140 μL, 2.256 mmol). The icebath was removed after 5 min and the reaction mixture was stirred at room temperature under argon for 12 h. Water was added and the product was extracted with methylene chloride (2×15 mL). The organic layers were washed with brine (1×2 mL) and dried over anhydrous sodium sulfate. The solid was filtered off and the filtrate was concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 40% ethyl acetate in hexanes yielded 2,4-dimethoxy-5-methoxymethyl-benzonitrile as a white solid (221 mg, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617346B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-3c1a480ddc8b4c1aa4f3df9902060f06 |
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| Source note | uspto-grants-2003_09 |
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