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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213799Generated: October 30, 2026

Sodium ethoxide → Ethyl 7-(2-chloroethoxy)-6-methoxy-3-nitro-2-naphthoate

https://huagongshe.com/reaction/2213799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant4-(2-Chloroethoxy)-5-methoxyphthalaldehydeHCID 11694418—
ReactantEthyl 3-nitropropionateHCID 11804910—
SolventEthanolHCID 702—
ProductEthyl 7-(2-chloroethoxy)-6-methoxy-3-nitro-2-naphthoateHCID 996846670%

Reaction Steps

To a solution of 2.43 g of ethyl 3-nitropropionate in 15 ml of absolute ethanol cooled using an ice bath, is added 20 mL of 1 N sodium ethoxide in ethanol dropwise over 10 minutes keeping the temperature at 0–5° C. A slurry of 4-(2-chloroethoxy)-5-methoxyphthalaldehyde in 5 mL of ethanol is added. The ice bath is removed and the reaction allowed to warm to room temperature and stirred for 16 hours. The reaction is transferred to a beaker with 300 mL of water and neutralized with acetic acid to pH 4. The solid is collected and washed first with water, then with 40 mL of cold ethanol. The solid is dried to provide 2.48 g (70%) of ethyl 7-(2-chloroethoxy)-6-methoxy-3-nitro-2-naphthoate and ethyl 6-(2-chloroethoxy)-7-methoxy-3-nitro-2-naphthoate (1:1 mixture) as a yellow solid, m.p. 119–29° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105531B2
Source datasetuspto-grants-2006_09
ORD IDord-62e34b94e1344b9f8baeb3ef8b22bc7e
Source noteuspto-grants-2006_09