HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602093Generated: November 1, 2026
4-Chlorobenzaldehyde → HCID 70024508, compound
https://huagongshe.com/reaction/1602093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Lysine ethyl ester dihydrochloride | HCID 107468 | — |
| Reactant | HCID 178465700 | HCID 178465700 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70024508 | HCID 70024508 | — |
Reaction Steps
N6-[1-(hydroxyimino)ethyl]-2-methyl-lysine, dihydrochloride ##STR8## EX-3A) A suspension of lysine ethyl ester dihydrochloride (33 g; 0.14 mole) and MgSO4 (34 g; 0.28 moles) in a solution of 4-chloro-benzaldehyde (39 g; 0.28 moles) and acetonitrile (500 mL) was stirred while N,N-diisopropylethylamine (36 g; 0.28 moles) was added in portions over 1/2 h. The mixture was stirred for 12 h, filtered, concentrated to a small volume, and diluted with 500 mL of diethyl ether. The ether solution was washed with 0.1% aqueous NaHCO3, aqueous 2 N NaOH containing 2 g/100 ml of NH2OH.HCl, again with 0.1% aqueous NaHCO3 and saturated aqueous NaCl. After drying with MgSO4 and removal of the solvent in vacuo, ethyl N, N'-di(4-chloro-phenylmethylene)-L-lysine was obtained as a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05981511 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-8837ba519e45434084a79dce854a57ce |
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| Source note | uspto-grants-1999_11 |
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