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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833493Generated: November 3, 2026

Acetone → Catechol

https://huagongshe.com/reaction/1833493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPhenolHCID 996—
ReactantPeracetic AcidHCID 6585—
ReactantAcetylacetoneHCID 31261—
ProductCatecholHCID 289—
ProductHydroquinoneHCID 785—

Reaction Steps

A reaction flask having an inner volume of 100 ml and provided with a thermometer, a stirrer, a reflux condenser and a dropping funnel was charged with 32.0 g (0.34 mol) of phenol and 0.0642 g (0.2 percent by weight based on said phenol) of acetyl acetone. To the contents of the flask, 7.6 g (0.034 mol) of an acetone solution of 34.0 percent by weight of peracetic acid was introduced introudced dropwise while under agitation at a temperature of 80° C over a period of 20 minutes. After the termination of said dropwise introduction of peracetic acid, the reaction system was agitated at the same temperature for an additional period of 42 minutes to bring the reaction to completion. Thereafter, the reaction mixture was analyzed for unaltered phenol and formed pyrocatechol and hydroquinone by gas chromatography. The results were 29.10 g, 1.66 g, and 1.09 g respectively. These values indicate the conversion of phenol to be 9.06 percent and the selectivity for dioxy-benzene to be 73.5 percent relative to peracetic acid and 81.2 percent relative to phenol. From the reaction mixture, acetone, formed acetic acid and acetyl acetone were simultaneously recovered by distillation. When the recovered mixture was analyzed for acetyl acetone by means of gas chromatography, the acetyl acetone content was found be 0.0591 g. This value indicates the recovery ratio to be 92 percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066707
Source datasetuspto-grants-1978_01
ORD IDord-481e162ed8644deca37c11150d998a22
Source noteuspto-grants-1978_01