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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243855Generated: October 31, 2026

Sodium ethoxide → HCID 21928991, compound

https://huagongshe.com/reaction/1243855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 69594764HCID 69594764—
SolventEthanolHCID 702—
ProductHCID 21928991HCID 219289914.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.3 g of ethyl 3-(2-oxo-5,5-diphenylcyclohex-3-enylamino)acrylate is dissolved in 6 cm3 of ethanol. The solution obtained is cooled to a temperature in the region of 0° C. 2 cm3 of sodium ethoxide solution (obtained from 0.23 g of sodium in 20 cm3 of ethanol) are added to the preceding solution at a temperature of between 0 and 5° C. After warming to a temperature in the region of 20° C., the resulting mixture is stirred for about 18 hours. About ten grams of crushed ice are then added to the reaction mixture and this mixture is then concentrated under reduced pressure (13 kPa) to half its volume. The mixture thus obtained is extracted five times with diethyl ether (three times 100 cm3, twice 50 cm3). The combined organic phases are successively washed with 100 cm3 and then 50 cm3 of saturated aqueous sodium chloride solution and then dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (13 kPa). The residue is purified by flash chromatography on a column of silica (eluent: cyclohexane/ethyl acetate (85/15 by volume)]. 0.013 g of ethyl 6,6-diphenyl-6,7-dihydro-1H-indole-3-carboxylate is thus obtained in the form of a yellow solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119115B2
Source datasetuspto-grants-2006_10
ORD IDord-835c7723e56e415a9114d0d7827784af
Source noteuspto-grants-2006_10