HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955251Generated: November 2, 2026
Methyl iodide → [5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-methyl-carbamic acid methyl ester
https://huagongshe.com/reaction/1955251
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-carbamic acid methyl ester | HCID 53935046 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [5-(2-Benzyloxy-ethoxy)-2-nitro-phenyl]-methyl-carbamic acid methyl ester | HCID 54555542 | 89% |
Reaction Steps
To a solution of [5-(2-benzyloxy-ethoxy)-2-nitro-phenyl]-carbamic acid methyl ester (2.03 g, 5.86 mmol) in anhydrous dimethylformamide (20 ml) was added iodomethane (1.82 ml, 29.3 mmol), followed by portion wise addition of NaH (0.35 g, 60%, 8.79 mmol). The reaction was stirred under nitrogen for 2 h. The reaction was quenched with NH4Cl (sat) (10 ml) and brine (10 ml), and the aqueous layer was extracted with ether (3×30 ml). The combined organics were dried over MgSO4, filtered and evaporated. The residue was chromatographed on silica gel eluting with hexanes, then 30% ethyl acetate/hexanes to give [5-(2-benzyloxy-ethoxy)-2-nitro-phenyl]-methyl-carbamic acid methyl ester (0.93 g, 89%) as an oil. Analysis calculated for C18H20N2O6 : C, 59.99; H, 5.59; N, 7.77. Found: C, 59.30; H, 5.34; N, 7.62.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06124323 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-2d6906aa0e4c491e9da7edaf8625f549 |
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| Source note | uspto-grants-2000_09 |
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