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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845796Generated: October 30, 2026

Ammonium Chloride → 2,3-Butanediamine, N,N'-dihydroxy-2,3-dimethyl-

https://huagongshe.com/reaction/1845796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2,3-Dimethyl-2,3-dinitrobutaneHCID 77577—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2,3-Butanediamine, N,N'-dihydroxy-2,3-dimethyl-HCID 8440218,376.1%

Reaction Conditions

Temperature9 °C

Reaction Steps

2,3-Dimethyl-2,3-dinitrobutane (82.56 g, 0.47 mmol) was dissolved in a mixture of THF (1407 mL) and water (235 mL). To this solution cooled to 8-10° C., Zn powder (126.9 g, 1.95 mol) was added in one portion. A solution of NH4Cl (202.1 g, 3.77 mol) in H2O (705 mL) was added dropwise to this slurry, with continued stirring for 1 h at 10° C., and the flask was stored in cooled water for 16 h. The slurry was filtered, and the precipitate was carefully washed with THF (4×200 mL). The precipitate was then dried by three washings with diethyl ether and collected. The solution was evaporated under vacuum until THF ceased to distill off. Then the solution was protected from air, and sodium carbonate (235 g) and sodium chloride (141 g) were added with cooling. Continuous extraction with chloroform (1880 mL) was performed over 18 h. The filtrate was concentrated to give oil product, then added petroleum ether to this mixture and stirred for 30 min at room temperature, filtered, dried, to afford a white powder (12.8 g, 18.4% yield). 1HNMR (400 MHz, DMSO): δ 6.89 (s, 1H), 5.34 (s, 1H), 0.96 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951766B2
Source datasetuspto-grants-2015_02
ORD IDord-1fc57bea1ca64b9cb9074daad25e09c0
Source noteuspto-grants-2015_02