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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417903Generated: November 3, 2026

Methanol → Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate

https://huagongshe.com/reaction/1417903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant8-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acidHCID 14756547—
ProductMethyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylateHCID 1098735849%

Reaction Steps

A mixture of 1-tetralon-7-carboxylic acid (7.0 g, 0.037 mol) in methanol (13.6 mL, 10.8 g, 0.30 mol) with a catalytic amount of hydrochloriic acid (0.07 mL, 0.12 g, 0.0012 mol) was stirred at reflux over 5 hours. The cooled reaction mixture was poured into ice water and extracted with ethyl acetate. The combined organic layers were backwashed with water and brine, dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The resulting solid was purified by flash chromatography using hexane:ethyl acetate::75:25. The resulting solid was triturated with hexane to give 1-tetralon-7-carboxylic acid methyl ester (3.61 g, 0.018 mol, 49%) as a yellow solid. mp=170°-172° C.; 1H NMR (CDCl3) d 8.7 (s, 1H), 8.15 (d, 1H, J=8.1 Hz), 7.35 (d, 1H, J=8.1 Hz), 3.95 (s, 3H), 3.05 (d, 2H, J=6.1 Hz), 2.7 (t, 2H, J=6.4 Hz), 2.15 (quintet, 2H, J=6.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05879657
Source datasetuspto-grants-1999_03
ORD IDord-b89152ce30af43bbbbb3ceca3903752c
Source noteuspto-grants-1999_03