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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-(2-Chloroethoxy)-5-methoxyphthalaldehyde | HCID 11694418 | — |
| Reactant | Ethyl 3-nitropropionate | HCID 11804910 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 7-(2-chloroethoxy)-6-methoxy-3-nitro-2-naphthoate | HCID 9968466 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105531B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-62e34b94e1344b9f8baeb3ef8b22bc7e |
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| Source note | uspto-grants-2006_09 |
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