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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62266Generated: October 26, 2026

p-Toluenesulfonic acid → (E)-5-bromo-6-methoxy-2-(3-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/62266

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
Reactant5-Bromo-6-methoxy-1-indanoneHCID 22278718—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(E)-5-bromo-6-methoxy-2-(3-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-oneHCID 117940380—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 11 (200 mg, 0.829 mmol) in toluene was added 3-(trifluoromethyl)benzaldehyde 99 (158.86 mg, 0.9128 mmol). PTSA (285.5 mg, 172.20 mmol) was added to the reaction mass, then stirred at 120° C. for 6 h, diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude compound 152 which was purified through flash chromatography by using 100-200 mesh silica gel. The compound (E)-5-bromo-6-methoxy-2-(3-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-one 152 was eluted at 30% ethyl acetate in hexane to afford yellow coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446047B2
Source datasetuspto-grants-2016_09
ORD IDord-ed88d7686de84dc78d827bbe9b44a619
Source noteuspto-grants-2016_09