HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279391Generated: November 2, 2026
Hydrochloric Acid → HCID 178497572, compound
https://huagongshe.com/reaction/1279391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Reactant | 2,3-Diaminobenzoic acid methyl ester | HCID 571825 | — |
| Reactant | 1-Acetylpiperidine-4-carbaldehyde | HCID 18428037 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178497572 | HCID 178497572 | 75% |
Reaction Steps
3.3 g (19.9 mmol) of methyl 2,3-diaminobenzoate were dissolved in 100 ml of methanol, and a solution of 4.0 g (25.8 mmol) of N-acetylpiperidine-4-carbaldehyde in 100 ml of methanol was added dropwise at room temperature. The whole was stirred for about 10 minutes at room temperature. Thereafter, 5.2 g (25.8 mmol) of copper(II) acetate, which was dissolved in 100 ml of water, were added dropwise and the whole was refluxed for 30 minutes. After cooling, 25 ml of concentrated hydrochloricacid were added carefully and the whole was again refluxed. 7.15 g (29.8 mmol) of sodium sulfide nonahydrate, dissolved in 100 ml of water, were then added dropwise and the whole was boiled for a further 10 minutes. After cooling, the reaction solution was evaporated down under reduced pressure. The residue obtained was dispersed in water and filtered. The filtrate was rendered alkaline with aqueous sodium bicarbonate solution and was extracted several times with ethyl acetate. The combined organic phases were washed with water, dried and evaporated down under reduced pressure. 4.5 g of the product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448271B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-b1ce59aa907e44b3842890e5c899b0b2 |
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| Source note | uspto-grants-2002_09 |
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