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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853798Generated: October 30, 2026

Water → 5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/853798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-2-(4-hydroxyphenyl)-1H-isoindole-1,3(2H)-dioneHCID 19793985—
SolventDimethylformamideHCID 6228—
Product5-Benzyloxy-2-(4-benzyloxyphenyl)isoindoline-1,3-dioneHCID 69471550186%

Reaction Steps

To 5-hydroxy-2-(4-hydroxyphenyl)isoindoline-1,3-dione (2.08 g) in DMF (20 mL) was added potassium carbonate (4.62 g) and a solution of benzyl bromide (3.07 g) in DMF (3.0 mL) dropwise under nitrogen atmosphere. The reaction was stirred at room temperature for 2 h then heated to 80° C. for 3 h. The mixture was cooled to room temperature, poured into water (250 mL) and let sit undisturbed for 2.0 h. The white solid was collected by filtration and washed with water. The solid was dried under high vacuum at 50° C. for 18 h yielding the title compound (3.30 g) as a white solid. 1H NMR (DMSO-d6): 7.87 (d, 1H, J=8.4 Hz), 7.48-7.35 (m, 12H), 7.32 (d, 2H, J=8.7 Hz), 7.13 (d, 2H, J=8.7 Hz), 5.35 (s, 2H), 5.17 (s, 2H); MS: 436 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256201B2
Source datasetuspto-grants-2007_08
ORD IDord-e63d17cc269a4f1fbad3885b5a44b3c6
Source noteuspto-grants-2007_08