HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395563Generated: October 25, 2026
Benzaldehyde → Bis-(hydroxyethyl)amino benzyl malonic acid
https://huagongshe.com/reaction/1395563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | Diethanolamine | HCID 8113 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Bis-(hydroxyethyl)amino benzyl malonic acid | HCID 70589253 | — |
Reaction Steps
Bis-(hydroxyethyl)amino benzyl malonic acid was prepared conventionally in a flask equipped with a stirrer and reflux condenser by first charging 0.1 mol of malonic acid, 0.1 mol of diethanol amine and 100 cc methanol. The contents were warmed to a temperature of about 20° C. and then 0.1 mol benzaldehyde were added to the flask and the reaction commenced. After refluxing the reaction mixture for 1 hour, the methanol was removed from the reaction mixture by coupling the flask to a vacuum source and heating to a temperature of about 50° C. The residue remaining in the flask then was triturated in acetone and the resulting acid isolated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04204062 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-d0712b297711489e8c21ef74542afd70 |
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| Source note | uspto-grants-1980_05 |
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