HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 650393Erstellt: 25. Oktober 2026
4-Bromoanisole → 1-(4-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid
https://huagongshe.com/reaction/650393
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Bromoanisole | HCID 7730 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate | HCID 18427631 | — |
| Edukt | Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate | HCID 18969641 | — |
| Edukt | HCID 178491912 | HCID 178491912 | — |
| Lösungsmittel | Ether tetrahydrofuran | HCID 21868444 | — |
| Produkt | 1-(4-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid | HCID 15908500 | 80% |
Reaktionsschritte
Ethyl (1RS) 1-Hydroxy-1-(methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indene-2-carboxylate, A solution of 4-bromoanisole (0.89 g, 5.0 mmol) in 9:1 Et2O/THF (10 ml) was added to magnesium turnings (0.105 g, 5.0 mmol), and the resulting mixture was allowed to stir for 30 min. The resultant 4-methoxyphenyl magnesium bromide was added dropwise to a solution of ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate (0.77 g, 2.4 mmol) in 10: 1 Et2O/ THF (55 ml) at 0° C. The resulting mixture was stirred at 0° C. for 1 h and was then partitioned between EtOAc and 1M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with 5% aqueous NaHCO3 and saturated aqueous NaCl and dried (MgSO4). The solvent was removed under reduced pressure, and the residue was purified by flash chromatography on silica gel, eluting with 10% EtOAc/hexanes to afford the title compound as a yellow glassy solid (0.80 g, 80%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06271399B1 |
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| Quelldatensatz | uspto-grants-2001_08 |
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| ORD ID | ord-3b93513ab0c946c19a9596f01a049c04 |
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| Quellennotiz | uspto-grants-2001_08 |
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