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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325522Generated: October 29, 2026

Sodium Hydroxide → HCID 178502885, compound

https://huagongshe.com/reaction/325522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactant2,6-Xylyl isocyanateHCID 98787—
ReactantHCID 178502882HCID 178502882—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178502885HCID 178502885—

Reaction Steps

To a suspension of 12.0 g. (0.11 mole) of methoxyguanidine hydrochloride in tetrahydrofuran (100 ml.) is added 8.8 g. (0.11 mole) of fifty percent (w/w) aqueous sodium hydroxide. After one hour of stirring, 5.0 g. of anhydrous sodium sulfate is added and the mixture is stirred for an additional hour. A solution of 14.7 g. (0.1 mole) of 2,6-dimethylphenylisocyanate in tetrahydrofuran (30 ml.) is added dropwise after which the mixture is stirred at room temperature overnight. 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 (4×100 ml.). The combined organic extracts are washed with water (1×50 ml.) dried over anhydrous magnesium sulfate and filtered. The filtrate is acidified with ethereal HCl and the solvents removed in vacuo to give a brown oil which is crystallized from acetonitrile to give 1-(2,6-dimethylphenyl)-3-methoxyamidinourea hydrochloride, m.p. 170°-1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440949
Source datasetuspto-grants-1984_04
ORD IDord-af174c15299546218d7ae7e74692db90
Source noteuspto-grants-1984_04