HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482661Generated: November 2, 2026
4-Nitrophenol → 1-[(2-methoxyethoxy)methoxy]-4-nitroBenzene
https://huagongshe.com/reaction/1482661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 1-[(2-methoxyethoxy)methoxy]-4-nitroBenzene | HCID 19609086 | 95.9% |
Reaction Steps
In a 50 mL, 3-neck RBF equipped with a magnetic stirrer, reflux condenser, calcium chloride guard tube and thermometer pocket were sequentially charged 4-nitrophenol (1.50 g), DIPEA (2.90 mL) and DCM (25 mL). MEM-Cl (2.016 g) was added drop wise to the reaction at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes and then allowed to stir at room temperature for 4 hours. The reaction was monitored on TLC using hexane:ethyl acetate (8:2) as mobile phase. After completion, the reaction was poured into water and the product was extracted in ethyl acetate and washed with brine. The organic layer was dried over sodium sulfate and the solvent was removed under reduced pressure to give 2.35 g of 1-[(2-methoxyethoxy)methoxy]-4-nitrobenzene as a solid, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09415049B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-5c994c2bb51347598683b2fd763a399e |
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| Source note | uspto-grants-2016_08 |
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