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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175294Generated: November 1, 2026

Ethylbenzene → HCID 59557708, compound

https://huagongshe.com/reaction/1175294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylbenzeneHCID 7500—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Bromo-2-chloro-4-(methoxycarbonyl)benzoic acidHCID 45480503—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59557708HCID 59557708—

Reaction Steps

To a solution of 5-bromo-2-chloro-4-(methoxycarbonyl)benzoic acid (1.21 g, 4.15 mmol) in dry dichloromethane (22.5 mL) was added dropwise oxalyl chloride (0.43 mL, 4.96 mmol) followed by N,N-dimethylformamide (1 mL). After being stirred for 2 h at room temperature, the reaction mixture was evaporated and the residue was dissolved in dry dichloromethane (20 mL) at room temperature under agron. After cooling to −5° C., ethylbenzene (0.46 g, 4.35 mmol) was added. Then AlCl3 (1.72 g, 12.8 mmol) was added portionwise and the reaction temperature was kept between −5° C. and 0° C. After being stirred at the same temperature for two hours, the reaction mixture was poured onto ice water and extracted with dichloromethane (100 mL). The combined organic layers were washed with 1 M HCl (60 mL), water (30 mL) and brine (60 mL), and dried over anhydrous Na2SO4 Concentration under reduced pressure provided the title compound as a yellow solid. Yield: 1.37 g (87%). 1H-NMR (CDCl3, 300 MHz): δ 7.89 (s, 1H), 7.72 (d, J=2.0 Hz, 1H), 7.70 (d, J=2.0 Hz, 1H), 7.64 (s, 1H), 7.33 (s, 1H), 7.30 (s, 1H), 3.98 (s, 3H), 2.70 (q, J=7.8 Hz, 2H), 1.27 (t, J=7.8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838498B2
Source datasetuspto-grants-2010_11
ORD IDord-6a6d94196ead4ded8097c86f683c5ec2
Source noteuspto-grants-2010_11