HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709325Generated: October 31, 2026
Nitric Acid → Ethyl 4-(4-acetyl-2-methoxy-5-nitrophenoxy)butanoate
https://huagongshe.com/reaction/709325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Ethyl 4-(4-acetyl-2-methoxyphenoxy)butanoate | HCID 60562321 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-(4-acetyl-2-methoxy-5-nitrophenoxy)butanoate | HCID 71143209 | 45.3% |
Reaction Steps
70% Nitric acid (60 mL) was cooled in an ice bath. Ethyl 4-(4-ethanoyl-2-methoxylphenoxy)butanoate (21 g, 0.075 mol) was added in portions over 20 minutes. The solution was stirred for 1.5 h while monitoring the temperature, which did not rise above 22° C. The solution was cautiously poured into water (800 mL), which was then cooled to 4° C. for several hours. The product was collected via filtration and recrystallized from ethanol (250 mL) to yield ethyl 4-(4-ethanoyl-2-methoxy-5-nitrophenoxy)butanoate (11.04 g, 45.3%) as a yellow flocculent powder. 1H NMR (δ, ppm): 1.31 (t, CO2CH2CH3), 2.21 (p, ArOCH2CH2CH2), 2.52 (s, ArCOCH3), 2.56 (t, ArOCH2CH2CH2), 3.98 (s, ArOCH3), 4.19 (m, ArOCH2 and CO2CH2), 6.76 (d, aromatic H ortho to ArOCH2), 7.65 (s, aromatic H ortho to ArOCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09180196B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-0339522a993844dd9271d2bad480cdb6 |
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| Source note | uspto-grants-2015_11 |
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