HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564840Generated: October 25, 2026
4-Ethoxyphenol → Methyl 3,5-dinitro4-(4-ethoxyphenoxy)benzoate
https://huagongshe.com/reaction/564840
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Ethoxyphenol | HCID 12150 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 4-chloro-3,5-dinitrobenzoate | HCID 96161 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3,5-dinitro4-(4-ethoxyphenoxy)benzoate | HCID 15462359 | 74% |
Reaction Steps
A mixture of 13 g (50 mmole) of methyl 4-chloro-3,5-dinitrobenzoate, 7.45 g (54 mmole) of 4-ethoxyphenol, and 13 ml of potassium hydroxide solution (3.03 g, 54 mmole) was heated under argon at 150° C. for 4 h. The mixture was cooled and partitioned between 130 ml of 2 N sodium hydroxide solution and 400 ml of dichloromethane. The organic layer was washed with 2×100 ml of saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated under high vacuum to give 14.5 g, which was chromatographed on a silica gel column (5 cm×50 cm), eluting with 25% hexane/75% dichloromethane to give 13.2 g (74% yield). TLC (silica gel, CH2Cl2), Rf0.80. NMR: 1H (300 MHz) (CDCl3) 1.39 (3H, t, —CH3); 3.97 (2H, q, —CH2—); 4.02 (3H, s, —OCH3); 6.81 (4H, s, arom); and 8.70 ppm (2H, s, arom).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169104A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-fecbf7bc60ad4590ae6e67f6ca22c7cb |
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| Source note | uspto-grants-2001_01 |
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