Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172172Generated: October 25, 2026

Ethanol → (6-Methoxy-indan-1-ylidene)-acetic acid ethyl ester

https://huagongshe.com/reaction/1172172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant6-Methoxy-1-IndanoneHCID 334036—
SolventDiethyl EtherHCID 3283—
Product(6-Methoxy-indan-1-ylidene)-acetic acid ethyl esterHCID 6704579647%

Reaction Conditions

Temperature70 °C

Reaction Steps

6-Methoxy-indan-1-one (5.02 g, 30.95 mmol) and triethyl phosphonoacetate (15.5 mL, 78.13 mmol) was dissolved in THF (20 mL) and added slowly to a mixture of EtOH (850 μL) and NaH (60% dispersion in oil, 2.5 g). The resulting slurry was stirred at 70° C. overnight. The crude mixture was diluted with diethyl ether and washed with water and brine, dried (Na2SO4), filtered and concentrated. The product was purified by silica gel flash column chromatography (5:1 hexanes in ethyl acetate) to afford (6-Methoxy-indan-1-ylidene)-acetic acid ethyl ester (3.18 g, 47%) as a mixture (˜1:1) of E/Z isomers. 1H NMR (400 MHz, CDCl3) mixture (˜1:1) of E/Z isomers δ 7.37 (d, 1H) 7.27 (d, 1H), 7.09 (d, 1H), 6.99 (dd, 1H), 6.97 (d, 1H), 6.81 (dd, 1H), 6.50 (m, 1H), 6.31-6.30 (m, 1H), 4.27 (quart, 2H), 4.22 (quart, 2H), 3.87 (s, 3H), 3.86 (s, 3H), 3.60 (m, 2H), 3.36-3.33 (m, 4H), 3.05-3.02 (m, 2H), 1.37 (t, 3H), 1.31 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834004B2
Source datasetuspto-grants-2010_11
ORD IDord-d57afd1c6d38473c813a2d8cb0ce3283
Source noteuspto-grants-2010_11