Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862339Generated: October 29, 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/862339

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl(1RS,3RS)-1,3-di-(3,4-methylenedioxyphenyl)indane-2-carboxylateHCID 18969665—
ReactantEthyl (RS)-1,3-Di-(3,4-methylenedioxyphenyl)indene-2-carboxylateHCID 21714780—
SolventMethanolHCID 887—
Product(1RS,3RS)-1,3-Di-(3,4-methylenedioxyphenyl)indane-2-carboxylic acidHCID 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 (5 ml 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716984
Source datasetuspto-grants-1998_02
ORD IDord-e0579b2b5f2c4bba8c2b1c2fba1a2b77
Source noteuspto-grants-1998_02