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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834848Generated: November 1, 2026

Acetone → 2-(N-isopropylamino)-4-methylbenzophenone

https://huagongshe.com/reaction/1834848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSulfuric AcidHCID 1118—
ReactantBorohydrideHCID 28123—
Reactant2-Amino-4-methylbenzophenoneHCID 78651—
SolventWaterHCID 962—
Product2-(N-isopropylamino)-4-methylbenzophenoneHCID 12898534—

Reaction Steps

Examples 1-19 as recorded in the following Table I represent trials in which the amount of 4-methyl-2-aminobenzophenone (a compound III in amount of 21.1 grs. or 0.1 mol) is held constant and the amount of other reaction system components including acetone (the compound III), borohydride (sodium borohydride), acid (sulfuric acid) and water are varied. In these examples, the reaction system is maintained at 20°-25° C. throughout the reaction and the rate of addition of the borohydride is controlled accordingly, such addition requiring in most cases about 60 minutes, after which the reaction system is stirred for an additional 60 minutes, followed by filtering. The filtrate is concentrated and the residue dissolved in about 88 mls. of heptane and the resulting solution extracted first with 20 mls. of 4N. ammonium hydroxide solution, then three times each with 10 mls. of 2N. sulfuric acid, and then washed with 10 mls. of 0.5N sulfuric acid. The heptane is distilled off to obtain the desired 2-(N-isopropylamino)-4-methylbenzophenone which boils at 180° -185° C./5 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071557
Source datasetuspto-grants-1978_01
ORD IDord-32188f8839f24aa4b6f0d833be52badb
Source noteuspto-grants-1978_01