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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229169Generated: October 25, 2026

Hydrochloric Acid → N-[4-(4-Methoxybenzoyl)phenyl]acetamide

https://huagongshe.com/reaction/229169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnisoleHCID 7519—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-Acetamidobenzoyl chlorideHCID 7010341—
SolventDichloromethaneHCID 6344—
ProductN-[4-(4-Methoxybenzoyl)phenyl]acetamideHCID 1349942045%

Reaction Conditions

Temperature0 °C

Reaction Steps

A round-bottomed flask was charged with 4-acetamidobenzoyl chloride (0.95 g, 4.57 mmol), anisole (0.60 mL, 5.48 mmoL) and CH2Cl2 (15 mL). Cooled in an ice bath, AlCl3 (0.93 g, 6.85 mmol) was added in portions. The mixture was stirred at 0° C. for 4 h. The resulting dark brown solution was poured into 1 N HCl (25 mL) with ice and the mixture was extracted with EtOAc (2×60 mL). The combined EtOAc extract was washed with water, brine, dried over Na2SO4, filtered, and the filtrate was concentrated to give brown solid. The crude product was purified by chromatography on a silica gel column eluted with hexanes:EtOAc (1:1) to give 0.55 g (45%) of compound 56 as light brown solid. mp 160-162° C. 1H NMR (400 MHz, CDCl3): δ 2.22 (s, 3H), 3.88 (s, 3H), 6.96 (d, J=8.8 Hz, 2H), 7.34 (br s, 1H), 7.55-7.65 (m, 2H), 7.77 (d, J=8.6 Hz, 2H), 7.79 (d, J=8.8 Hz, 2H). LCMS (ESI): m/z 270 (M+H)+, 268 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560589B2
Source datasetuspto-grants-2009_07
ORD IDord-d28c7ddfda8749a68ffbe33011d17e8d
Source noteuspto-grants-2009_07