HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074444Generated: October 26, 2026
Methyl iodide → 4-[1-(Methoxymethyl)-propyl]nitrobenzene
https://huagongshe.com/reaction/1074444
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(4-Nitrophenyl)butanol | HCID 20496692 | — |
| Reactant | Monopotassium phosphate dipotassium phosphate | HCID 21889592 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[1-(Methoxymethyl)-propyl]nitrobenzene | HCID 20496699 | — |
Reaction Steps
To a mixture of 2.2 g of sodium hydride (as a 50% oil dispersion) and 15.5 g of methyl iodide in 300 ml of dried dimethylformamide, there was added dropwise a solution of 7.1 g of 2-(4-nitrophenyl)butanol in 100 ml of dimethylformamide. The resulting mixture was stirred at room temperature for 20 hours and then poured into an aqueous solution containing 0.2 M potassium hydrogen phosphate/potassium dihydrogen phosphate buffer solution (pH 7). The resulting mixture was extracted several times with diethyl ether and the combined organic extracts were washed with aqueous dilute sodium thiosulfate solution, water, and aqueous saturated sodium chloride solution, and dried over magnesium sulfate. Evaporation of the solvent gave a red oil which was purified by chromatography on silica gel and elution with ethyl acetate/hexane to give 4-[1-(methoxymethyl)-propyl]nitrobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04391818 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-5b2cd17d5b0d4b1ca0ab484f102606a9 |
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| Source note | uspto-grants-1983_07 |
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