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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789113Generated: October 28, 2026

3-(Dimethylamino)-1-phenyl-1-propanone → alpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride

https://huagongshe.com/reaction/1789113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Dimethylamino)-1-phenyl-1-propanoneHCID 77042—
Reactant2,4,6-TriisopropylbenzenesulphonohydrazideHCID 359333—
Reactantalpha-(1-Methyl-2-pyrrolidinyl)acetophenone hydrochlorideHCID 20133696—
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 of a white solid melting at 210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686309
Source datasetuspto-grants-1987_08
ORD IDord-e86a3e9ff2604fdf978a729dc5841fcf
Source noteuspto-grants-1987_08