HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27242Generated: October 29, 2026
Carbon Dioxide → HCID 70592850, compound
https://huagongshe.com/reaction/27242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | HCID 12413922 | HCID 12413922 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70592850 | HCID 70592850 | 94% |
Reaction Steps
38.4 g (0.19 mol) of 2-dichloromethyl-phenyl isocyanate are allowed to run into a suspension of 135 g (0.43 mol) of Ba(OH)2 ×8H2O in 500 ml of water, at 15°-18° C. whilst stirring vigorously (with the aid of a baffle and an impeller stirrer). The mixture is stirred for a further 30-40 minutes at this temperature and about 95 ml of 10% strength hydrochloric acid are added dropwise to the reaction mixture, at 3°-5° C., until the pH is 5-6, CO2 being evolved. After the evolution of CO2 has subsided, the reaction mixture is rendered alkaline with 4 ml of 50% strength NaOH. After removing the external cooling bath, 25 g (0.25 mol) of acetylacetone are then allowed to run in dropwise in the course of 15-30 minutes and the mixture is stirred for a further 4-6 hours at room temperature. It is then filtered and the filter residue is taken up in methanol and warmed to 40° C. After cooling, the undissolved barium salt is filtered off and the filtrate is evaporated. After drying in a desiccator, 33 g (94% of theory) of 3-acetyl-3-hydroxy-quinaldine with a melting point of 54°-56° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04220779 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-6f81b4f6fca2443abd1a1a0498cdccda |
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| Source note | uspto-grants-1980_09 |
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