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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853800Generated: November 1, 2026

5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline → 5-Hydroxy-2-(4-hydroxyphenyl)isoindoline

https://huagongshe.com/reaction/853800

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-2-(4-benzyloxyphenyl)isoindolineHCID 69472856—
SolventTrifluoroacetic acidHCID 6422—
Product5-Hydroxy-2-(4-hydroxyphenyl)isoindolineHCID 6947292042.6%

Reaction Steps

5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline (400 mg) in TFA (12 mL) was refluxed under nitrogen atmosphere for 1 h and cooled. The solvents were removed under vacuum. The residue was dissolved in ethyl acetate (100 mL) and washed with saturated sodium bicarbonate (twice) then brine. Purification by chromatography on silica gel (eluant: dichloromethane—methanol 95:5) gave the title compound (95 mg) as a tan solid. 1H NMR (DMSO-d6): 9.35 (s, 1H), 8.53 (s, 1H), 7.14 (d, 1H, J=8.4 Hz), 6.75 (s br, 1H), 6.69 (m, 3H), 6.49 (d, 2H, J=8.7 Hz), 4.38 (m, 4H); MS: 228 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256201B2
Source datasetuspto-grants-2007_08
ORD IDord-7290c3167f08488eb813835ec1c34f46
Source noteuspto-grants-2007_08