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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364693Generated: October 29, 2026

Benzaldehyde → HCID 54486151, compound

https://huagongshe.com/reaction/364693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantGlycineHCID 750—
SolventWaterHCID 962—
ProductHCID 54486151HCID 54486151—

Reaction Steps

In the process of this invention, there is no particular limitation on the sequence of charging the starting materials, the solvent, and the other materials. For example, an organic solvent having dissolved therein glycine, water and the aldehyde and optionally the phase transfer catalyst are charged, and with stirring, the alkali as a solid or an aqueous solution is charged or added dropwise to perform the reaction. Alternatively, it is possible to dissolve glycine in water and the alkali, and then add dropwise a solution of the benzaldehyde and the surface-active agent in an organic solvent to perform the reaction. Another method comprises charging or dropwise adding the alkali as a solid or aqueous solution into or to a mixture of glycine, water, the benzaldehyde, the organic solvent and the surface active agent, thereby performing the reaction. The reaction may be carried out at a temperature of 0° to 80° C. for 1 to 50 hours, preferably 10° to 60° C. for 3 to 30 hours. In this manner, the alkali metal or alkaline earth metal salt of the N-benzylidene-β-phenylserine is formed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04605759
Source datasetuspto-grants-1986_08
ORD IDord-ca0f4bd7de914dddb985f9f8a022bb3d
Source noteuspto-grants-1986_08