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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649592Generated: October 30, 2026

Sodium Hydroxide → HCID 178436235, compound

https://huagongshe.com/reaction/1649592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactant2,6-Diethylphenyl isothiocyanateHCID 141193—
ReactantHydrochloride methanolHCID 21893726—
ReactantHCID 178485188HCID 178485188—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178436235HCID 178436235107.2%

Reaction Steps

To a stirred suspension of 7.3 g (30.0 mmol) of methylguanidine sulfate in THF (100 ml) was added 4.8 g (60.0 mmol) of 50% W/W aqueous NaOH. The mixture was stirred for one hour after which 5.0 g of anhydrous Na2SO4 was added and the mixture stirred for an additional hour. To the mixture was added dropwise over one hour a solution of 5.7 g (30.0 mmol) of 2,6-diethylphenylisothiocyanate in THF (40 ml) and the mixture was stirred for two hours at ambient temperature. The THF was removed under vacuum and the residue partitioned between H2O and CHCl3. The layers were separated and the aqueous layer extracted with CHCl3 (1×100 ml). The extracts were dried (MgSO4) and concentrated to give a yellow oil which was dissolved in MeOH and acidified with HCl/MeOH. The MeOH was removed under vacuum to give a viscous yellow oil which slowly crystallized on standing. Crystallization from MeOH/CH3C≡N gave 8.5 g (94 %) of the desired salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04418209
Source datasetuspto-grants-1983_11
ORD IDord-1f1a965371ba4b68a4bd60bb9349b903
Source noteuspto-grants-1983_11