HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834848Generated: November 1, 2026
Acetone → 2-(N-isopropylamino)-4-methylbenzophenone
https://huagongshe.com/reaction/1834848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | 2-Amino-4-methylbenzophenone | HCID 78651 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(N-isopropylamino)-4-methylbenzophenone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04071557 |
|---|
| Source dataset | uspto-grants-1978_01 |
|---|
| ORD ID | ord-32188f8839f24aa4b6f0d833be52badb |
|---|
| Source note | uspto-grants-1978_01 |
|---|