HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081247Generated: November 3, 2026
Hydrochloric Acid → 1-(4-Chlorophenyl)-5-(2-methoxyethoxy)-4-oxo-1,4-dihydrocinnoline-3-carboxylic acid
https://huagongshe.com/reaction/2081247
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Methoxyethanol | HCID 3015637 | — |
| Reactant | Methyl 5-chloro-1-(4-chlorophenyl)-4-oxo-1,4-dihydrocinnoline-3-carboxylate | HCID 10904198 | — |
| Product | 1-(4-Chlorophenyl)-5-(2-methoxyethoxy)-4-oxo-1,4-dihydrocinnoline-3-carboxylic acid | HCID 10915750 | 98% |
Reaction Steps
A solution of 255 g of potassium hydroxide (3.9 moles, pellets, 85+%) in 3.2 1 of methoxyethanol was stirred at 45° C. as 450 g of solid methyl phenylcinnoline-carboxylate (1.29 moles) from step 3 was added in portions. The reaction vessel was fitted with a distillation head and placed under reduced pressure (approx. 40 mmHg). The reaction was heated at 50° C. for 1 hr., then at 65° C. for 1 hr. to distill off methanol and some methoxyethanol (total volume removed 280 ml). The distillation head was replaced with a reflux condenser and the reaction was heated between 90° C. and 110° C. for 1 hr. The reaction was allowed to cool to 50° C. before the addition of 1 liter of water and was cooled to 25° C. before the resulting slurry was poured into 4 1 of a cold 0.8 N hydrochloric acid solution (3.1 moles HCl). The resulting precipitate was isolated by filtration, washed with water (2×2 1), and dried under reduced pressure at 50° C. to give 472 g (98%) of an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05183891 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-272a59a85a1e44b88b67d5ba51fdfcd1 |
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| Source note | uspto-grants-1993_02 |
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