HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650404Generated: October 28, 2026
ethyl(1RS,3RS)-1,3-di-(3,4-methylenedioxyphenyl)indane-2-carboxylate → (1RS,3RS)-1,3-Di-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid
https://huagongshe.com/reaction/650404
Participants
| Role | Name | HCID | Charge |
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| Reactant | ethyl(1RS,3RS)-1,3-di-(3,4-methylenedioxyphenyl)indane-2-carboxylate | HCID 18969665 | — |
| Reactant | Ethyl (RS)-1,3-Di-(3,4-methylenedioxyphenyl)indene-2-carboxylate | HCID 21714780 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1RS,3RS)-1,3-Di-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid | HCID 10135727 | — |
Reaction Steps
Ethyl (1RS,3RS)-1,3-Di-(3,4-methylenedioxy-phenyl)indane-2-carboxylate. Ethyl(RS)-1,3-di-(3,4-Methylenedioxyphenyl)indene-2-carboxylate (163 mg, 0.38 mmol) was placed in MeOH (0.05 ml), and to this was added SmI2 (10 ml of 0.1M solution in THF, 1.0 mmol). The resulting mixture was stirred under an argon atmosphere overnight, at which time thin layer chromatographic analysis indicated that the reaction was incomplete. Additional SmI2 (5ml of 0.1M solution in THF, 0.5 mmol) was added, and stirring was continued for 2 h. The reaction mixture was partitioned between Et2O and 5% aqueous Na2S2O3. The organic extract was washed with saturated aqueous NaCl and dried (MgSO4). The solvent was removed under reduced pressure, and the residue was purified by flash chromatography, eluting with 10% EtOAc/ hexanes to afford the title compound as a colorless, glassy solid (120 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271399B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-129d2a21e642475380c3203df4867b9b |
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| Source note | uspto-grants-2001_08 |
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