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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682515Generated: November 4, 2026

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

https://huagongshe.com/reaction/1682515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
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

Part A--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 hydrochloric 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 numberUS05635477
Source datasetuspto-grants-1997_06
ORD IDord-d9cb39208a8444cd902fc7de5bd00cc6
Source noteuspto-grants-1997_06