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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482663Generated: October 30, 2026

Hydrazine hydrate (1:1) → 2-Hydrazino-5,5-Dimethyl-1,3-Diazacyclohex-2-ene Monohydrochloride

https://huagongshe.com/reaction/482663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Nitroamino5,5-dimethyl-1,3-diazacyclohex-2-eneHCID 20245345—
Solvent1-PropanolHCID 1031—
Product2-Hydrazino-5,5-Dimethyl-1,3-Diazacyclohex-2-ene MonohydrochlorideHCID 20245351—

Reaction Conditions

Temperature95 °C

Reaction Steps

Hydrazine hydrate (1.98 grams; 0.0396 mole) is added to a mixture of 1-propanol (50 mls), ammonium chloride (1.56 grams; 0.028 mole), and 2-nitroamino5,5-dimethyl-1,3-diazacyclohex-2-ene (5.0 grams; 0.029 mole). The resulting mixture is heated to 95° C. over a period of 20 minutes, and stirred thereat for 2 hours. Additional hydrazine hydrate (0.94 gram; 0.0187 mole) is then added to the reaction mixture, and heating at 95° C. is continued for an additional 24 hours. The slurry is then cooled to room temperature and the precipitate is isolated by filtration, washed with 1-propanol (20 mls) and dried under a vacuum at 50° C. to obtain 3.55 grams (68.5% of theoretical) of the desired product. Evaporation of the filtrate affords a second crop (1.5 grams) of the same compound. The total yield in two crops is 96.5% of theoretical. The infrared absorption spectra of the two crops are identical with that of 2-hydrazino-5,5-dimethyl-1,3-diazacyclohex-2ene monohydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04574155
Source datasetuspto-grants-1986_03
ORD IDord-07f7e5893e064b4baf4102007f18bd67
Source noteuspto-grants-1986_03