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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100044Generated: October 31, 2026

Water → (4-Bromophenyl)(4-hydroxy-2-methylphenyl)methanone

https://huagongshe.com/reaction/2100044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant(4-Bromophenyl)[2-methyl-4-(methyloxy)phenyl]methanoneHCID 11023132—
SolventBenzeneHCID 241—
Product(4-Bromophenyl)(4-hydroxy-2-methylphenyl)methanoneHCID 68654122123.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of (4-bromophenyl)[2-methyl-4-(methyloxy)phenyl]methanone (27) (1.12 g, 3.67 mmoL) in benzene (25 mL) was added AlCl3 (1.98 g, 14.85 mmol). The mixture was heated at 90° C. for 3 h. Upon cooling, water (25 mL) was added, and the mixture was extracted with Et2O. The organics were dried with MgSO4 and concentrated. The crude material was purified by chromatography on silica gel (EtOAc:hexanes) to yield 1.32 g (86%) of compound 28. 1H NMR (400 MHz, DMSO-d6): δ 2.26 (s, 3H), 6.63 (dd, J=2.4 Hz, 8.4 Hz, 1H), 6.72 (d, J=2.2 Hz, 1H), 7.18 (d, J=8.4 Hz, 1H), 7.55 (d, J=8.4 Hz, 2H), 7.70 (d, J=8.4 Hz, 2H), 10.10 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569601B2
Source datasetuspto-grants-2009_08
ORD IDord-3e6a42bcbff644f4a6444bd981f8e255
Source noteuspto-grants-2009_08