Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842352Generated: October 27, 2026

Sodium Bicarbonate → Benzylamide tetrasodium salt

https://huagongshe.com/reaction/842352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl amideHCID 22619318—
Solvent1,4-DioxaneHCID 31275—
ProductBenzylamide tetrasodium saltHCID 86757958—

Reaction Steps

Subsequently, to the above benzylamide of S1 anhydride (157 mg) were added a sodium bicarbonate aqueous solution (NaHCO3 110 mg, water 20 mL) and 1,4-dioxane (20 mL), and the resultant was allowed to undergo a reaction at room temperature for 16 hours. After the reaction was completed, the solvent was removed under reduced pressure to afford benzylamide tetrasodium salt of S1 compound (196 mg). The 1H-NMR and IR data of this compound were as shown below. From these data, the compound thus obtained was confirmed to be a derivative in which the carboxyl groups bonded t the saturated carbon atoms in the structural formula S1 compound were benzylamidated) while other carboxyl groups were substituted with sodium salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372943B1
Source datasetuspto-grants-2002_04
ORD IDord-46a7c8b5e41d4f04b971fe04ee4b9ef1
Source noteuspto-grants-2002_04