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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252363Generated: November 2, 2026

Sulfuric Acid → Methyl 2-oxo-3-phenylpropanoate

https://huagongshe.com/reaction/1252363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantButyl phenylpyruvateHCID 18979724—
SolventO-XyleneHCID 7237—
ProductMethyl 2-oxo-3-phenylpropanoateHCID 562359—

Reaction Steps

Following the procedure of step (iii) of Example 1 but charging 1 g of sulfuric acid into the three-necked flask in lieu of p-toluenesulfonic acid monohydrate, and the whole o-xylene solution containing 95 g (0.43 mole) of butyl phenylpyruvate and sulfuric acid as obtained in step (ii) of Example 8 into the dropping funnel in place of methyl phenylpyruvate, the reaction was carried out in the same manner as in step (iii) of Example 1. The total reaction time was prolonged to 6 hours. The conversion of butyl phenylpyruvate was 97 percent and the selectivity toward butyl α-acetamidocinnamate 85 mole percent (yield of butyl α-acetamidocinnamate: 93 g). The reaction mixture was washed with water in the same manner as in step (iii) of Example 1 to give about 650 ml of an o-xylene solution containing butyl α-acetamidocinnamate in a concentration of about 0.55 mole per liter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743547
Source datasetuspto-grants-1988_05
ORD IDord-a13ffb120bc5464c8ce0b259a06ae5bb
Source noteuspto-grants-1988_05