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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299196Generated: October 30, 2026

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

https://huagongshe.com/reaction/2299196

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, 1), 7.2 (s, 1H), 7.35 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495560B1
Source datasetuspto-grants-2002_12
ORD IDord-0e0cb656a40f44b0b3218516c3088ed3
Source noteuspto-grants-2002_12