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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014642Generated: October 25, 2026

(2,6-Dimethylphenyl)methanol → 2-(2-(3-(2,6-Dimethylbenzyloxy)phenoxy)ethyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1014642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,6-Dimethylphenyl)methanolHCID 186748—
Reactant2-[2-(3-Hydroxy-phenoxy)-ethyl]-isoindole-1,3-dioneHCID 58027534—
Product2-(2-(3-(2,6-Dimethylbenzyloxy)phenoxy)ethyl)isoindoline-1,3-dioneHCID 67317099—

Reaction Steps

Mitsunobu reaction of phenol 24 with 2,6-dimethylbenzyl alcohol gave 2-(2-(3-(2,6-dimethylbenzyloxy)phenoxy)ethyl)isoindoline-1,3-dione as yellow oil. Yield (1.2 g, 85%): 1H NMR (400 MHz, CDCl3) δ 7.85-7.88 (m, 2H), 7.71-7.74 (m, 2H), 7.12-7.18 (m, 1H), 7.01-7.10 (m, 3H), 6.60 (dd, J=8.0, 1.8 Hz, 1H), 6.57 (s, 1H), 6.51 (dd, J=8.0, 1.8 Hz, 1H), 4.99 (s, 2H), 4.09-4.24 (m, 4H), 2.38 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982071B2
Source datasetuspto-grants-2011_07
ORD IDord-28253cea154d453e9e0d31f55865ba20
Source noteuspto-grants-2011_07