HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444201Generated: October 29, 2026
Sodium Hydroxide → 1-Ethyl-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid
https://huagongshe.com/reaction/444201
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-ethyl-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate | HCID 12876363 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Ethyl-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylic acid | HCID 12876364 | 40.3% |
Reaction Steps
Sodium hydroxide (1.6 g) was dissolved in 30 ml of water, and 2 g of ethyl 1-ethyl-4,5-dioxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate was added, and the mixture was stirred at 90° C. for 2 hours. The insoluble matter was removed, and the filtrate was adjusted to pH 1 with dilute hydrochloric acid under ice cooling. The crystals that precipitated were collected by filtration to afford 0.72 g of the captioned product. The product had a melting point of 212° to 214° C. (uncorrected). The infrared absorption spectrum (KBr tablet method) of the product had maximum absorptions at 3460, 2960, 1740, 1710, 1640 and 1495 cm-1. The nuclear magnetic resonance spectrum (CF3COOH, 60 Mc, TMS) had signals at δ1.70 (3H, t, J=7.5 Hz), 2.2-2.75 (2H, m), 2.8-3.2 (2H, m), 3.3-3.65 (2H, m), 4.64 (2H, q, J=7.5 Hz) and 9.30 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04263302 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-c51c5db44ff943bb9c3b7903a597e610 |
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| Source note | uspto-grants-1981_04 |
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