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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989354Generated: October 31, 2026

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

https://huagongshe.com/reaction/989354

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 1N 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 numberUS06638929B2
Source datasetuspto-grants-2003_10
ORD IDord-a26690e421fc4e409a0aaf37b84eed63
Source noteuspto-grants-2003_10