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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757560Generated: October 29, 2026

Hydrochloric Acid → HCID 54490552, compound

https://huagongshe.com/reaction/1757560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannous chloride dihydrateHCID 61436—
ReactantHCID 19388496HCID 19388496—
SolventEthanolHCID 702—
ProductHCID 54490552HCID 5449055277.6%

Reaction Steps

To a mixture of 4 ml of conc. hydrochloric acid and 4 ml of ethanol was added 622 mg (2.0 mmol.) of methyl 4-(2-nitrobenzyl)-1-piperazinecarbodithioate. The mixture was chilled withice, and then to this chilled mixture was dropwise added under stirring a solution of 2.7 g (12 mmol.) of SnCl2.2H2O in 5 ml of ethanol for 15 min. After the addition was complete, the mixture was further stirred at room temperature for 2 hours. Ethanol was distilled off under reduced pressure, and to the residue were added 10 ml of water and 10 ml of ethyl acetate. The resulting mixture was made alkaline by addition of saturated aqueous sodium hydrogen carbonate solution. Precipitated insolubles were removed by filtration. The organic filtrate was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and placed under reduced pressure to distill off the solvent. The residue was crystallized from ether, and collected by filtration, yielding 436 mg of the desired compound as a white crystallineproduct, m.p. 110°-113.5° C., yield 77.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446146
Source datasetuspto-grants-1995_08
ORD IDord-19d37c75b22941fdb0e806efac9055f5
Source noteuspto-grants-1995_08