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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105610Generated: November 2, 2026

Benzaldehyde → HCID 6453905, compound

https://huagongshe.com/reaction/1105610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDiethyl EtherHCID 3283—
ReactantMethyl L-ornithine dihydrochlorideHCID 14273060—
SolventDichloromethaneHCID 6344—
ProductHCID 6453905HCID 6453905204.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Approximately 6.8 kg of ornithine methyl ester dihydrochloride is suspended in 10 l of methylene chloride, cooled to 0° C. and 6.5 kg of benzaldehyde, dissolved in 10 l of methylene chloride, is added at such a rate as to maintain the reaction temperature at 0° to -5° C. The reaction mixture is allowed to warm to room temperature, stirring continued for an additional 2 hours, and 20 l of diethyl ether added thereto. Upon standing overnight, the triethylammonium hydrochloride that precipitates is removed by filtration, and the precipitate is washed with an additional 6.8 liters of diethyl ether. The combined filtrates are evaporated in vacuo and the residue dissolved in 34 l of diethyl ether. The organic solution is washed four times with 4 l of water, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to yield 9.28 kg of dibenzaldimine ornithine methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309442
Source datasetuspto-grants-1982_01
ORD IDord-f01d0d29849c4349b76f95189cca5275
Source noteuspto-grants-1982_01