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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41432Generated: October 26, 2026

(2,4-Bis-benzyloxy-5-trifluoromethyl-phenyl)-(1,3-dihydro-isoindol-2-yl)-methanone → (1,3-Dihydro-isoindol-2-yl)-(2,4-dihydroxy-5-trifluoromethyl-phenyl)-methanone

https://huagongshe.com/reaction/41432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,4-Bis-benzyloxy-5-trifluoromethyl-phenyl)-(1,3-dihydro-isoindol-2-yl)-methanoneHCID 59263097—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(1,3-Dihydro-isoindol-2-yl)-(2,4-dihydroxy-5-trifluoromethyl-phenyl)-methanoneHCID 11955511100.5%

Reaction Steps

A solution of (2,4-bis-benzyloxy-5-trifluoromethyl-phenyl)-(1,3-dihydro-isoindol-2-yl)-methanone (140 mg, 0.28 mmol) in methanol (5 mL) was hydrogenated at atmospheric pressure over 10% palladium on charcoal (34 mg) for 4 hours. A further portion of catalyst was added (31 mg) and hydrogenation continued for a further 1.5 hours. The mixture was filtered through Celite, eluting with methanol, then the filtrate was concentrated in vacuo to afford the title compound as a white solid (91 mg, quant.). 1H NMR (DMSO-d6) 10.79 (1H, s), 10.70 (1H, s), 7.40-7.35 (2H, m), 7.31-7.35 (3H, m), 6.61 (1H, s), 4.79 (2H, br.s), 4.68 (2H, br.s). MS: [M+H]+ 324.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530469B2
Source datasetuspto-grants-2013_09
ORD IDord-a7b167db5c4144dea20ebfc267421d17
Source noteuspto-grants-2013_09