Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626832Generated: October 31, 2026

Acetyl chloride → 1-(4-Bromo-5-chloro-2-hydroxyphenyl)ethanone

https://huagongshe.com/reaction/626832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Bromo-1-chloro-4-methoxybenzeneHCID 24212081—
SolventCarbon DisulfideHCID 6348—
Product1-(4-Bromo-5-chloro-2-hydroxyphenyl)ethanoneHCID 5956417799.3%

Reaction Steps

The 2-bromo-1-chloro-4-methoxybenzene (25.0 g, 113 mmol) [Oakwood cat#035670] was dissolved in carbon disulfide (250 mL), and the acetyl chloride (12 mL, 170 mmol) and aluminum trichloride (37.6 g, 282 mmol) were added. The reaction was heated to reflux and monitored by LC/MS. After heating for 1 h, the reaction became two layers. The reaction allowed to cool to room temperature and poured over ice. The slurry was extracted with ethyl acetate 3×, the combined organic layer was washed with brine, dried over magnesium sulfate and concentrated to give 1-(4-bromo-5-chloro-2-hydroxyphenyl)ethanone as a solid (28.0 g, 99%). 1H NMR (300 MHz, CDCl3) δ 12.12 (s, 1H), 7.78 (s, 1H), 7.31 (s, 1H), 2.62 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309251B2
Source datasetuspto-grants-2016_04
ORD IDord-f0f7c87820114e84b606c4a4a374221e
Source noteuspto-grants-2016_04