HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457546Generated: October 29, 2026
Imidazole → [1-(3-Chlorophenyl)-2-nitroethoxy]triethylsilane
https://huagongshe.com/reaction/457546
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Chlorotriethylsilane | HCID 13819 | — |
| Reactant | HCID 11413010 | HCID 11413010 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [1-(3-Chlorophenyl)-2-nitroethoxy]triethylsilane | HCID 22021350 | 91% |
Reaction Steps
To a solution of 1-(3-chlorophenyl)-2-nitro-ethanol (26 g, 0.14 mol) in DMF (50 mL) were added imidazole (28.6 g, 0.42 mol) and chlorotriethylsilane (25.3 g, 0.17 mol). The reaction mixture was stirred at room temperature for 2 h. After quenching with water, the mixture was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over Na2SO4, and filtered. After removal of solvent, the crude product was purified by flash chromatography (2% EtOAc/hexane) to yield the title compound (37 g, 91%) as a colorless oil. 1H NMR (300 MHz, CDCl3) δ 7.40 (1H, s), 7.27–7.32 (3H, m), 5.40 (1H, dd, J=3.2, 9.5 Hz), 4.51 (1H, dd, J=9.5, 12.1 Hz), 4.36 (1H, dd, J=3.3, 12.1 Hz), 0.85 (9H, t, J=7.5 Hz), 0.54 (6H, q, J=7.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189716B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-4d5e17c6555e4869acaef063adb7b9e5 |
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| Source note | uspto-grants-2007_03 |
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