Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092435Generated: November 2, 2026

Ethylbenzene → (5-Chloro-2-hydroxyphenyl)(4-ethylphenyl)methanone

https://huagongshe.com/reaction/1092435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylbenzeneHCID 7500—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Chloro-o-anisic acidHCID 76970—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(5-Chloro-2-hydroxyphenyl)(4-ethylphenyl)methanoneHCID 5774111271%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A solution of 2-methoxy-5-chlorobenzoic acid (2.0 g, 10.5 mmol) in dry CH2Cl2 (10 mL) was stirred at room temperature under agron. Oxalyl chloride (2.0 g, 15.8 mmol) was added dropwise to the reaction mixture followed by DMF (0.04 mL). After stirring overnight, the volatiles were evaporated using a rotary evaporator and the residue was dissolved in dry CH2Cl2 (10 mL) at room temperature under agron. After cooling to −5° C., ethylbenzene (2.57 mL, 21 mmol) was added, followed by portionwise addition of AlCl3 (2.80 g, 21 mmol) while maintaining the reaction temperature between −5° C. and 0° C. The reaction mixture was stirred for 4 h at room temperature, and then poured into ice water and extracted with CH2Cl2 (50 mL×2). The organic layer was then washed with 1N HCl (50 mL), 1N NaOH (50 mL), water (50 mL) and brine (50 mL) and dried over anhydrous Na2SO4. The filtrate was concentrated and the crude product was purified by column chromatography (PE:EA=10:1) to give the target compound (1.944 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129434B2
Source datasetuspto-grants-2012_03
ORD IDord-42bee6de9b444d489f1e075ac4ea2956
Source noteuspto-grants-2012_03