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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242013Generated: October 31, 2026

Hydrazine → HCID 58914783, compound

https://huagongshe.com/reaction/2242013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantAcetonitrile methylene chlorideHCID 21877088—
ReactantHCID 58914781HCID 58914781—
SolventEthanolHCID 702—
ProductHCID 58914783HCID 5891478387%

Reaction Steps

The Pthalimido Pyrrole 4 (1 eq) was dissolved in ethanol and hydrazine (3 eq) at room temperature under nitrogen. Upon heating to reflux, the reaction generated a white precipitate. Stir at reflux until complete (−2 h) by TLC(CH2Cl2/acetonitrile (95:5 v/v), the UV active product was at Rf=0.2) and LCMS. Upon reaching completion, the reaction was allowed to cool to room temperature and the precipitate was vacuum-filtered off using a medium to fine cintered-glass filter. The filtrate was concentrated under reduced pressure to a gummy solid. The crude material was taken up in ethanol/EtOAc (1:1 v/v), stirred and the precipitate was filtered off in the same fashion as before. The filtrate was concentrated under reduced pressure and than dried in vacuo for 10-15 min. This process of adding ethanol/EtOAc, filtering and concentrating was done one more time or as needed to remove the majority of the white precipitate and residual hydrazine. The product was then dried in vacuo overnight. The material was used without further purification. Once dried, the reaction yielded the product as a glass (−87% yield over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671049B2
Source datasetuspto-grants-2010_03
ORD IDord-d20d37d2149740738f22f461f7573ea2
Source noteuspto-grants-2010_03