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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696482Generated: October 31, 2026

Ethanol → Ethyl 3-nitro-1-naphthoate

https://huagongshe.com/reaction/1696482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Nitro-1-naphthoic acidHCID 230772—
ProductEthyl 3-nitro-1-naphthoateHCID 22262323—

Reaction Steps

To a solution of 3-nitronaphthalene-1-carboxylic acid (4.34 g, 20 mmol) in EtOH (50 mL) was added SOCl2 (3.70 mL, 30 mmol) at 0° C. The mixture was heated at reflux for 2 h and then concentrated. The residue was recrystallized from EtOH to yield ethyl 3-nitronaphthalene-1-carboxylate (4.2 g). 1H NMR (300 MHz, DMSO-d6): δ 9.16 (s, 1H), 8.77 (d, J=8.7 Hz, 1H), 8.62 (s, 1H), 8.34 (d, J=8.1 Hz, 1H), 7.87 (t, J=7.2 Hz, 1H), 7.75 (t, J=7.2 Hz, 1H), 4.43 (q, J=7.2 Hz, 2H), 1.38 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163756B2
Source datasetuspto-grants-2012_04
ORD IDord-21d51a0db3434959be02f22173f077fb
Source noteuspto-grants-2012_04