Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995761Generated: November 1, 2026

Sodium Methoxide → Sodium Sulfate

https://huagongshe.com/reaction/1995761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantCarbamimidamidomethanimidamideHCID 176517607—
ReactantImidodicarbonimidic diamide sulfateHCID 176518576—
SolventMethanolHCID 887—
ProductSodium SulfateHCID 24436—
ProductCarbamimidamidomethanimidamideHCID 176517607—

Reaction Steps

Biguanide was prepared fresh by refluxing anhydrous biguanide sulfate in a methanol solution of freshly prepared sodium methylate by the method of Slotta et al. (Slotta, K. H., Tschesche, R., Ber. Dtsch. Chem. Ges. 1929, B62, 1390-1398). The biguanide was used in solution as prepared for all of the reactions. Because sodium sulfate formed in the preparation of biguanide did not interfere with subsequent reactions, it was not necessary to separate it from the biguanide. Ethyl malonamate used in the preparation of Ib (see Example 1 below) was prepared as follows by methods of Galat and Marguery (Galat, A., J. Am. Chem. Soc. 1948, 70, 2596 and Marguery, M. F., Bull. Soc. Chem. France 1905, 33, 541; J. Recherces Centr. Natl. Recherche Sci., Labs. Bellevue (Paris) 1959, 47, 147), through Chem. Abstr. 1962, 56, 4744 g.): Diethyl malonate was converted to the mono-potassium salt of the half-ester. The latter was converted to ethyl malonyl chloride, which in turn was reacted with anhydrous ammonia in ice-cold ether to form ethyl malonamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04405806
Source datasetuspto-grants-1983_09
ORD IDord-4c099983db854446aee79575b894e996
Source noteuspto-grants-1983_09