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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845168Generated: October 25, 2026

Water → beta-Dimethylamino-alpha-methylpropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride

https://huagongshe.com/reaction/845168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-(Dimethylamino)-2-methylpropiophenone hydrochlorideHCID 199992—
Reactant2,4,6-TriisopropylbenzenesulphonohydrazideHCID 359333—
Reactantbeta-Dimethylamino-alpha-methylpropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazoneHCID 86741736—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Productbeta-Dimethylamino-alpha-methylpropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochlorideHCID 86741737—

Reaction Steps

β-Dimethylamino-α-methylpropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone can be prepared as follows: 2,4,6-triisopropylbenzenesulphonylhydrazine (23.8 g) is added to α-methyl-β-dimethylaminopropiophenone hydrochloride (16.3 g) dissolved in methylene chloride (150 cc) and acetic acid (5 cc). The solution is stirred at ambient temperature for 24 hours and is then poured into water (50 cc). The aqueous phase is extracted with methylene chloride (2×50 cc) and then the organic phases are combined, dried over magnesium sulphate, filtered and evaporated to dryness under reduced pressure (2.7 kPa) at 40° C. to give a yellow oil which is crystallised in a mixture (120 cc) of ethyl acetate and isopropyl ether (50/50 by volume). In this way β-dimethylamino-α-methylpropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride (16 g) is obtained in the form of a white solid melting at 147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04755599
Source datasetuspto-grants-1988_07
ORD IDord-b7e1fd274eea4215aee66863b0f7e084
Source noteuspto-grants-1988_07