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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26025Generated: October 30, 2026

Sodium Hydroxide → HCID 178436841, compound

https://huagongshe.com/reaction/26025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactant2,6-Diethyl-4-nitrophenylisocyanateHCID 20383631—
ReactantHydrochloride methanolHCID 21893726—
ReactantHCID 178485188HCID 178485188—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178436841HCID 178436841—

Reaction Steps

To a stirred suspension of 7.3 g (30.0 mmol) of methylguanidine sulfate in tetrahydrofuran (80 ml) is added 4.8 g (60.0 mmol) of 50% w/w sodium hydroxide in water with continued stirring for one hour. Anhydrous sodium sulfate (10.0 g) is added and the mixture stirred an additional hour after which 6.6 g (30.0 mmol) of 2,6-diethyl-4-nitrophenylisocyanate is added and the resulting mixture stirred at room temperature over-night. The tetrahydrofuran is removed under vacuum and the residue partitioned between water and chloroform. The layers are separated and the aqueous layer extracted with chloroform (1 × 100 ml). The combined extracts are dried (MgSO4) and concentrated to give a yellow foam which is dissolved in methanol and acidified with HCl/MeOH. The methanol is removed under vacuum to give a yellow viscous oil which solidifies on scratching. Crystallization from methanol-ethyl acetate gives 1-(2,6-diethyl-4-nitrophenyl)-3-methylamidinourea hydrochloride as a pale yellow solid, m.p. 173°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147804
Source datasetuspto-grants-1979_04
ORD IDord-328eb0e795b2461abdd4d2bc8141f4f8
Source noteuspto-grants-1979_04