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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579228Generated: October 26, 2026

Hydrazine, (phenylmethyl)-, hydrochloride (1:1) → 1-Benzyl-2-(1-methylsulfonyl-2-propylidene)hydrazine monohydrochloride

https://huagongshe.com/reaction/579228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, (phenylmethyl)-, hydrochloride (1:1)HCID 14084—
Reactant1-(Methylsulphonyl)acetoneHCID 78695—
SolventMethanolHCID 887—
Product1-Benzyl-2-(1-methylsulfonyl-2-propylidene)hydrazine monohydrochlorideHCID 86689346102.8%

Reaction Steps

To a 50 ml volume three-necked flask, 1-methylsulfonyl-2-propanone (7-2-1) (2.01 g), methanol (10 ml) and benzylhydrazine monohydrochloride (14-c) (2.56 g) were added under a nitrogen atmosphere at room temperature, then additional methanol (10 ml) was added. The resulting reaction mixture was stirred at room temperature for three days, and filtered to give the primary crystal. The filtrate was concentrated under reduced pressure, and filtered again to give the crystal. The crystal was combined with the primary crystal to give 4.2 g of 1-benzyl-2-(1-methylsulfonyl-2-propylidene)hydrazine monohydrochloride (5-2-3). Additionally, the hydrochloride (5-2-3) (0.28 g) was dissolved in saturated aqueous sodium hydrogen carbonate solution (5.0 ml), and extracted with tert-butyl methyl ether (5.0 ml) 2 times. Then, the organic layer was concentrated under reduced pressure to give 0.22 g of 1-benzyl-2-(1-methylsulfonyl-2-propylidene)hydrazine (5-2-3′). NMR data of Compound (5-2-3′) is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040709B2
Source datasetuspto-grants-2015_05
ORD IDord-1c9f760c7b8744f6aac0a9cbbfe97638
Source noteuspto-grants-2015_05