HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26025Generated: October 30, 2026
Sodium Hydroxide → HCID 178436841, compound
https://huagongshe.com/reaction/26025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 2,6-Diethyl-4-nitrophenylisocyanate | HCID 20383631 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 178485188 | HCID 178485188 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178436841 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04147804 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-328eb0e795b2461abdd4d2bc8141f4f8 |
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| Source note | uspto-grants-1979_04 |
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