HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576140Generated: October 30, 2026
Ethyl Acetate → 1-(2-(Benzyloxy)ethoxy)-4-nitro-2-(trifluoromethyl)benzene
https://huagongshe.com/reaction/576140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | 2-Fluoro-5-nitrobenzotrifluoride | HCID 94954 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-(Benzyloxy)ethoxy)-4-nitro-2-(trifluoromethyl)benzene | HCID 90418319 | 76% |
Reaction Steps
To a mixture of 1-fluoro-4-nitro-2-(trifluoromethyl)benzene (5 g, 23.91 mmol) in DMF (50 mL) was added K2CO3 (6.61 g, 47.8 mmol) and 2-(benzyloxy)ethanol (4.00 g, 26.3 mmol) at rt. The mixture was stirred at 110° C. for 12 h. LCMS and TLC (PE/EA=5:1, Rf=0.4) showed the reaction was finished. The mixture was filtrated, and the filtrate was concentrated to give crude product, which was purified by silica gel column to obtain 1-(2-(benzyloxy)ethoxy)-4-nitro-2-(trifluoromethyl)benzene (7.1 g, 18.18 mmol, 76.0% yield): 1H NMR (400 MHz, CDCl3) 8.49 (d, J=2.4 Hz, 1H), 8.38 (d, J=9.2 Hz, 1H), 7.54-7.28 (m, 5H), 7.13 (d, J=8.4 Hz, 1H), 4.56 (s, 2H), 4.36 (t, J=4.8 Hz, 2H), 3.89 (t, J=3.6 Hz, 2H); ES-LCMS m/z 342 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035063B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-5044aa23fe964960af138eb3cf015031 |
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| Source note | uspto-grants-2015_05 |
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