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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650742Generated: October 25, 2026

Triethylsilane → 1-(4-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acid

https://huagongshe.com/reaction/650742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantBoronHCID 5462311—
Reactant1-Hydroxy-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)-indene-2-carboxylateHCID 18427688—
SolventDichloromethaneHCID 6344—
Product1-(4-Methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxylic acidHCID 15908500—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl (1R)2R)-1-hydroxy-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)-indene-2-carboxylate (0.80 g, 1.9 mmol) in CH2Cl2 (10 ml) at 0° C. under an argon atmosphere was added triethylsilane (0.28 a, 2.4 mmol), followed by boron tritluoride etherate (1 ml, 8.1 mmol). The resulting solution was stirred at 0° C. for 10 min, and was then partitioned between EtOAc and 3M HCl. The organic extract was washed with saturated aqueous NaCl and dried (MgSO4). The solvent was removed in vacun, and the residue was filtered through a pad of silica gel, eluting with CH2Cl2. The title compound (mixture of Δ1 and Δ2 double bond isomers) was obtained as a glassy, yellow solid (0.72 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274737B1
Source datasetuspto-grants-2001_08
ORD IDord-8b5eb771d1c74507bb1912415c17a641
Source noteuspto-grants-2001_08