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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511915Generated: November 3, 2026

Water → HCID 53244623, compound

https://huagongshe.com/reaction/511915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantPerbenzoic acidHCID 523077—
ReactantHCID 86675009HCID 86675009—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 53244623HCID 5324462375.7%

Reaction Conditions

Temperature-18 °C

Reaction Steps

8.6 g (67 mmol) of 2-(ethoxycarbonyloxy)benzoyl chloride (obtained in Example 1.2) and 10.2 g (44 mmol) of benzenecarboperoxoic acid are dissolved in 43 ml of chloroform. The mixture is cooled to −18° C. and then 2.2 ml (38 mmol) of pyridine in 5 ml of dichloromethane are added dropwise. After stirring at −18° C. for 2 hours, water is added and the mixture is extracted with dichloromethane. The organic phase is dried over magnesium sulphate, filtered and then concentrated. The residue is purified by chromatography on silica gel eluted with a pentane/dichloromethane 5/5 mixture. 11 g of (2-(ethoxycarbonyloxy)benzoyl)benzoyl peroxide are obtained in the form of a beige solid with a yield of 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102607B2
Source datasetuspto-grants-2015_08
ORD IDord-2df086326bd64c78acdd05ad96490f62
Source noteuspto-grants-2015_08