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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743189Generated: November 3, 2026

Water → 1-(4-isopropylphenyl)propan-1-one

https://huagongshe.com/reaction/1743189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCumeneHCID 7406—
ReactantPropionyl chlorideHCID 62324—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventCarbon DisulfideHCID 6348—
Product1-(4-isopropylphenyl)propan-1-oneHCID 3773435112.1%

Reaction Steps

Propionyl chloride (11.6 g, 125 mmol) was dropwise added to a suspension of aluminium chloride (16.7 g, 125 mmol) and cumene (18.0 g, 150 mmol) in carbon disulfide (30 mL) at −5° C., and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into water with ice, and the organic layer was separated, washed with an aqueous saturated sodium hydrogencarbonate and water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to obtain 1-(4-isopropylphenyl)propan-1-one (24.7 g). Sodium borohydride (1.29 g, 34.2 mmol) was added to a solution of the thus-obtained compound (13.0 g, 68.4 mmol) in ethanol (80 mL) with cooling with ice, and the mixture was stirred for 30 minutes at room temperature. Water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to obtain the title compound (11.5 g, yield 79%). This was oily.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008950B1
Source datasetuspto-grants-2006_03
ORD IDord-b1f79aea01404e119cf3860db12f89a4
Source noteuspto-grants-2006_03