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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514109Generated: October 25, 2026

Sulfuric Acid → 1-(4-Bromophenyl)propan-2-one

https://huagongshe.com/reaction/514109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantEthyl 4-(4-bromophenyl)-3-methylbut-2-enoateHCID 67126147—
Product1-(4-Bromophenyl)propan-2-oneHCID 736332—
Product7-Bromo-3-methylnaphthalen-1-olHCID 67126282—

Reaction Conditions

Temperature50 °C

Reaction Steps

A flask containing the crude ethyl 4-(4-bromophenyl)-3-methylbut-2-enoate from above (˜30 grams) was treated with concentrated H2SO4 (120 mL) and warmed to 50° C. for 2.5 h. The reaction was poured onto ˜500 mL of crushed ice. Once the ice had thawed, the brown suspension was extracted with two portions of EtOAc (500 mL and 100 mL, respectively). The two extracts were combined, washed with saturated NaHCO3, dried (MgSO4), filtered, and concentrated to ˜55 mL. The residue was treated with DCM and wet-loaded onto a silica gel column and purified by flash chromatography (ethyl acetate/hexanes) giving the desired product (16.6 g, 60% yield over 2 steps from 1-(4-bromophenyl)propan-2-one. 1H NMR (400 MHz, CDCl3) δ 8.29 (d, J=1.9 Hz, 1H), 7.57 (d, J=8.6 Hz, 1H), 7.50 (dd, J=8.6, 2.0 Hz, 1H), 7.17 (s, 1H), 6.67 (s, 1H), 2.42 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102614B2
Source datasetuspto-grants-2015_08
ORD IDord-46eeb4e8af464da3816ed035a3e94581
Source noteuspto-grants-2015_08