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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288154Generated: October 30, 2026

Hydrochloric Acid → 1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylic acid

https://huagongshe.com/reaction/2288154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylsilaneHCID 12052—
ReactantEthyl(RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindene-2-carboxylateHCID 18969642—
ReactantEthyl(1RS)-1-Hydroxy-1-(3,4-methylenedioxyphenyl)-3-phenylindene-2-carboxylateHCID 18969644—
SolventDichloromethaneHCID 6344—
Product1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylic acidHCID 21714790100%

Reaction Steps

Ethyl (RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindene-2-carboxylate. To a solution of ethyl (1RS)-1-hydroxy-1-(3,4-methylenedioxyphenyl)-3-phenylindene-2-carboxylate (1.03 g, 2.58 mmol) in CH2Cl2 (40 mL) was added triethylsilane (0.49 ml, 3.07 mmol), followed by boron trifluoride etherate (1.55 ml, 12.6 mmol). The reaction mixture was allowed to stir for 15 min, at which time was added slowly 3 M HCl. The mixture was extracted with EtOAc. The organic extract was washed successively with H2O, 5% aqueous NaHCO3 and saturated aqueous NaCl. The solvent was removed in vacuo to provide the title compound (1.00 g, 100%) as a mixture of Δ1 and Δ2 double bond isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087389
Source datasetuspto-grants-2000_07
ORD IDord-98b370ab6d7146c9a0bb38e2d894a094
Source noteuspto-grants-2000_07