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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199797Generated: October 27, 2026

(E)-2-(3-bromo-2,6-difluorobenzylidene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one → 2, 6-difluorobenzyl-6-methoxy-5-morpholino-2, 3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/2199797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-2-(3-bromo-2,6-difluorobenzylidene)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-oneHCID 117940382—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2, 6-difluorobenzyl-6-methoxy-5-morpholino-2, 3-dihydro-1H-inden-1-oneHCID 117940026—

Reaction Steps

The 41 (40 mg, 0.088 mmol) was dissolved in methanol 15 mL and added Pd/C 20 mg and stirred under hydrogen balloon for 6 h. The reaction was filtered through elite bed and washed with excess methanol. The organic layer was concentrated to get the crude compound 42, which was purified by flash chromatography using 100-200 mesh silica gel. The compound 2-(2,6-difluorobenzyl)-6-methoxy-5-morpholino-2,3-dihydro-1H-inden-1-one 42 was eluted as des-brominated compound at 26% ethyl acetate in hexane as half white coloured solid. 1HNMR (400 MHz, CDCl3) δ ppm 7.17 (m, 2H), 6.89 (m, 3H), 3.89 (m, 7H), 3.35 (m, 1H), 3.19 (m, 4H), 3.06 (m, 2H), 2.76 (m, 2H); MS (ESI) m/z 374.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359315B2
Source datasetuspto-grants-2016_06
ORD IDord-4490921ab13c466d9fcaaa93a40bf801
Source noteuspto-grants-2016_06