HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899953Generated: October 29, 2026
Sulfuric acid magnesium salt (1:1) → HCID 55251614, compound
https://huagongshe.com/reaction/899953
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 4-Quinolinecarboxaldehyde | HCID 78072 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 2-aminoisobutyrate hydrochloride | HCID 13258034 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 55251614 | HCID 55251614 | 25.7% |
Reaction Steps
A mixture of 1.5 g of methyl α-aminoisobutyrate hydrochloride and 1.4 ml of triethylamine in 30 ml of dichloromethane is stirred at 0° C. for 20 minutes. Next, 1 g of magnesium sulfate and 1.5 g of quinoline-4-carbaldehyde are added. Stirring is continued for 15 hours at room temperature and the mixture is then concentrated under reduced pressure. The residue is taken up in 35 ml of methanol and the solution obtained is cooled to 0° C. 0.4 g of sodium borohydride is added portionwise and stirring is continued at room temperature for 15 hours. The precipitate formed is filtered and the filtrate is concentrated under reduced pressure. The residue obtained is purified by recrystallization from diisopropyl ether. 600 mg of the expected product are obtained in the form of a pink oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354933B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-027ed2065b8f46449de3cc20d5e9fa14 |
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| Source note | uspto-grants-2008_04 |
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