Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369225Generated: November 1, 2026

Ethyl bromoacetate → Ethyl (+/-) 3-(3-methoxyphenyl)indeneacetate

https://huagongshe.com/reaction/1369225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant3-(3-Methoxyphenyl)indeneHCID 15621211—
ReactantHCID 178418261HCID 178418261—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (+/-) 3-(3-methoxyphenyl)indeneacetateHCID 1834068619.8%

Reaction Steps

To a cold solution of 3-(3-methoxyphenyl)indene (4 g, 18 mmol), prepared by the method of J. Med. Chem. 1981, 24, 998, in THF (15 mL) at 0° C. was added dropwise a solution of LiN(TMS)2 (20 mL, 1M in THF) over 5 min. The resulting solution was added dropwise to a solution of ethyl bromoacetate (3.34 g, 20 mmol) in THF (15 mL) at −78° C. over 30 min. After 2.5 h, the mixture was quenched with saturated ammonium chloride solution and the layers were separated. The organic layer was dried over MgSO4 and concentrated to give the crude product which was purified by column chromatography (SiO2/2-4% EtOAc/hexane) to give title compound (1.1 g): 1H NMR (400 MHz, CDCl3) δ1.30 (t, 3H), 2.50 (m, 1H), 2.85 (m, 1H), 3.85 (s, 3H), 4.0 (m, 1H), 4.20 (q, 2H), 6.6 (s, 1H), 6.9 (m, 1H), 7.2 (s, 1H), 7.35 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576643B2
Source datasetuspto-grants-2003_06
ORD IDord-cd6d004a51dc44aa8dfe57f92813c043
Source noteuspto-grants-2003_06