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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845166Generated: October 25, 2026

2,4,6-Triisopropylbenzenesulphonohydrazide → alpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride

https://huagongshe.com/reaction/845166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TriisopropylbenzenesulphonohydrazideHCID 359333—
Reactantalpha-(1-Methyl-2-pyrrolidinyl)acetophenone hydrochlorideHCID 20133696—
Reactantbeta-Dimethylaminopropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazoneHCID 86741729—
Reactantalpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazoneHCID 86741735—
Productalpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochlorideHCID 86741734—

Reaction Steps

α-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone can be prepared by a method similar to that described in Example 22 for the preparation of β-dimethylaminopropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone, but starting from 2,4,6-triisopropylbenzenesulphonylhydrazine (30.6 g) and α-(1-methyl-2-pyrrolidinyl)acetophenone hydrochloride (28.3 g). In this way, α-(1-methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride (31.1 g) is obtained in the form a white solid melting at 210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04755599
Source datasetuspto-grants-1988_07
ORD IDord-04bf7de5a05d404b8d0f79c21b09b904
Source noteuspto-grants-1988_07