Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55002Generated: October 26, 2026

Diethyl Ether → 2-(2,4-Diethylbenzoyl)benzoic acid

https://huagongshe.com/reaction/55002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPhthalic AnhydrideHCID 6811—
Reactant1,3-DiethylbenzeneHCID 8864—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1,1,2-TetrachloroethaneHCID 12418—
Product2-(2,4-Diethylbenzoyl)benzoic acidHCID 1995715393%

Reaction Steps

To a cooled mixture of phthalic anhydride (50 g, 0.34 mol) and aluminum chloride (99 g) in tetrachloroethane (300 mL) was added dropwise 1,3-diethylbenzene (50 g) over 11/4 hours. The mixture was stirred in an ice bath for 30 minutes, additional tetrachloroethane was added, and the mixture was stirred for 2 hours. The reaction mixture was poured into concentrated HCl/ice (1 L), ether (500 mL) was added and the mixture was filtered. The organic layer was separated, washed with saturated Na2CO3 (6×), the basic layer was extracted with CH2Cl2 and the CH2Cl2 layer was extracted with 2N NaOH and the 2N NaOH layer was acidified. The basic layer was acidified with aqueous HCl, this acidic layer was combined with the above acidified 2N NaOH layer and the mixture was extracted with ether. The CH2Cl2 layer and the ether layer were combined and concentrated in vacuo. The residue was slurried with water, filtered and rinsed with hexane to afford 88.8 g (93%) of 2-(2,4-diethylbenzoyl)benzoic acid, m.p. 115°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624922
Source datasetuspto-grants-1997_04
ORD IDord-6cc04374b2914c638e36d02d78689a42
Source noteuspto-grants-1997_04