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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 8-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid | HCID 14756547 | — |
| Product | Methyl 8-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate | HCID 10987358 | 49% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05635477 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-d9cb39208a8444cd902fc7de5bd00cc6 |
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| Source note | uspto-grants-1997_06 |
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