HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386436Generated: October 25, 2026
4-Methoxyphenol → Ethyl 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoate
https://huagongshe.com/reaction/1386436
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Ethyl 2-fluoro-6-[3,4-(methylenedioxy)phenoxy]benzoate | HCID 15540783 | — |
| Reactant | Sodium 4-methoxyphenolate | HCID 23679016 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoate | HCID 15540784 | — |
| Product | Sodium 4-methoxyphenolate | HCID 23679016 | — |
Reaction Steps
Sodium 4-methoxyphenoxide was prepared as described in part A using 4-methoxyphenol (156 mg, 1.25 mmol) and was dried in vacuo. A solution of ethyl 2-fluoro-6-[3,4-(methylenedioxy)phenoxy]benzoate (304 mg, 1.0 mmol) in DMSO was added to the sodium 4-methoxyphenoxide at 25° C. and the mixture was stirred until all the solid had dissolved (approximately 20 min.). Stirring was continued at 25° C. for an additional 24 hr. The reaction mixture was then warmed to 60° C. and stirred for 2 hr., then stirred for 4 hr. at 80° C. At this time all of the ethyl 2-fluoro-6-[3,4-(methylenedioxy)phenoxy]benzoate had been consumed, as judged by thin layer chromatography (TLC). The reaction was cooled to 25° C., diluted with water (10 ml) and extracted with EtOAc (3×10 ml). The organic extract was washed with water (2×7 ml) and brine (7 ml), dried (MgSO4) and concentrated to give a light yellow oil. The crude product was purified by flash chromatography (SiO2, 50% CH2Cl2/hexane—CH2Cl2) giving 195 mg of ethyl 2-(4-methoxyphenoxy)-6-[3,4-(methylenedioxy)phenoxy]benzoate. (47% yield, m.p. 84.5-85° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265428B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-6dfd9872ce9645348c7608553fabbe93 |
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| Source note | uspto-grants-2001_07 |
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