Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417680Generated: November 1, 2026

Ethanol → Ethyl 6-bromonaphthalene-2-carboxylate

https://huagongshe.com/reaction/1417680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant6-Bromo-2-naphthalenecarboxylic acidHCID 4549852—
ProductEthyl 6-bromonaphthalene-2-carboxylateHCID 1249959—

Reaction Steps

To a solution of 6-bromo-2-naphthalenecarboxylic acid (Compound M) 3.1 g, (12.43 mmol) in ethanol (30 ml, 23.55 g, 511.0 mmol) was added 18M sulfuric acid (2 ml). The solution was refluxed for 30 minutes, cooled to room temperature, and the reaction mixture partitioned between pentane (100 ml) and water (100 ml). The aqueous phase was extracted with pentane (100 ml) and the combined organic layers washed with saturated aqueous NaCl (100 ml), dried (MgSO4), and concentrated to yield an off-white solid. Purification by flash chromatography (silica, 10% EtOAc-hexane) afforded the title compound as a white solid. 1H NMR (CDCl3): δ 8.58 (1H, br s), 8.10 (1H, dd, J=1.7, 9 Hz), 8.06 (1H, d, J=2 Hz), 7.83 (1H, d, J=9 Hz), 7.80 (1H, d, J=9 Hz), 7.62 (1H, dd, J=2, 9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877207
Source datasetuspto-grants-1999_03
ORD IDord-2a4e953117814ae2be6e2c6524199a61
Source noteuspto-grants-1999_03