HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650749Generated: October 29, 2026
Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate → 1-(3-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid
https://huagongshe.com/reaction/650749
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(3,4-methylenedioxyphenyl)1-oxoindene-2-carboxylate | HCID 18427631 | — |
| Reactant | HCID 178490745 | HCID 178490745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid | HCID 15908502 | 124.6% |
Reaction Steps
To a solution of ethyl 3-(3,4-methylenedioxyphenyl)-1-oxoindene-2-carboxylate (100 mg, 0.31 mmol) in THF (2 ml) under an argon atmosphere at 0° C. was added a solution of freshly prepared 3-methoxyphenyl magnesium bromide (0.31 mmol). After stirring for 15 min, additional 3-methoxyphenyl magnesium bromide (0.06 mmol) was added. Stirring was continued for 45 min, at which time thin layer chromatographic analysis indicated that the reaction was incomplete. Additional 3-methoxyphenyl magnesium bromide (0.12 mmol) was added. After stirring for 2 h more, the mixture was partitioned between 3M HCl and EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3, H2O and saturated aqueous NaCl. The solvent was removed in vacuo, and the residue was purified by flash chromatography, eluting with 15% EtOAc/hexanes to afford the title compound (150 mg, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274737B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-c71d19b58d5447f5816cfb9bf6fe4d86 |
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| Source note | uspto-grants-2001_08 |
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