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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62243Generated: October 26, 2026

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

https://huagongshe.com/reaction/62243

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-Chloro-2-(trifluoromethyl)benzaldehydeHCID 17750758—
Reactant6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-oneHCID 117940128—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(E)-2-(5-chloro-2-(trifluoromethyl)benzylidene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-oneHCID 117940155—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 13 (100 mg, 0404 mmol) in toluene 5 mL was added 5-chloro-2-(trifluoromethyl)benzaldehyde 51 (84.4 mg, 0.404 mmol) and PTSA (153.9 mg, 0.809 mmol). The reaction was stirred at 120° C. for 6 h. The reaction mixture was 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 52. The crude 52 was purified through flash chromatography by using 100-200 mesh silica gel. The compound (E)-2-(5-chloro-2-(trifluoromethyl)benzylidene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 52 was eluted at 28% 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-62d4719d80604e709b80dd79588b42f4
Source noteuspto-grants-2016_09