Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199835Generated: October 29, 2026

(E)-5-chloro-6-methoxy-2-(4-((trifluoromethyl)thio)benzylidene)-2,3-dihydro-1H-inden-1-one → 5-chloro-6-methoxy-2-(4-((trifluoromethyl)thio)benzyl)-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/2199835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-5-chloro-6-methoxy-2-(4-((trifluoromethyl)thio)benzylidene)-2,3-dihydro-1H-inden-1-oneHCID 117940130—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product5-chloro-6-methoxy-2-(4-((trifluoromethyl)thio)benzyl)-2,3-dihydro-1H-inden-1-oneHCID 117940046—

Reaction Steps

The compound 171 (85 mg, 0.195 mmol) was dissolved in methanol 25 mL and Pt/C (40 mg) and the reaction stirred under H2 balloon for 6 h. The reaction was filtered through celite bed and washed with excess methanol. The organic layer was concentrated to get the crude. The crude was purified by flash chromatography using 100-200 mesh silica gel. The compound was eluted at 25% ethylacetate in hexane as half white coloured solid 172. 1H NMR (400 MHz, CDCl3) δ ppm 7.57 (d, 2H), 7.43 (s, 1H), 7.27 (d, 2H), 7.25 (s, 1H), 3.94 (s, 3H), 3.37 (dd, 1H), 3.11 (m, 1H), 2.99 (m, 1H), 2.72 (m, 2H); MS-ES+386.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359315B2
Source datasetuspto-grants-2016_06
ORD IDord-fec7c58b01614df3a7870f749a1c72c7
Source noteuspto-grants-2016_06