Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74344Generated: October 26, 2026

4-Benzyloxy-1-butanol → 2-(3-(3-(4-(Benzyloxy)butoxy)phenyl)propyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/74344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-1-butanolHCID 562212—
Reactant2-[3-(3-Hydroxyphenyl)propyl]isoindole-1,3-dioneHCID 58027542—
Product2-(3-(3-(4-(Benzyloxy)butoxy)phenyl)propyl)isoindoline-1,3-dioneHCID 67316104—

Reaction Steps

Mitsunobu reaction of phenol 58 with 4-benzyloxybutanol gave 2-(3-(3-(4-(benzyloxy)butoxy)phenyl)propyl)isoindoline-1,3-dione as yellow oil. Yield (0.830 g, 54%): 1H NMR (400 MHz, CDCl3) δ 7.81-7.85 (m, 2H), 7.70-7.74 (m, 2H), 7.28-7.35 (m, 5H), 7.10-7.16 (m, 1H), 6.77 (d, J=8.2 Hz, 1H), 6.73 (s, 1H), 6.65 (dd, J=7.6, 2.4 Hz, 1H), 4.52 (s, 2H), 3.94 (t, J=6.0 Hz, 2H), 3.74 (t, J=7.2 Hz, 2H), 3.55 (t, J=6.4 Hz, 2H), 2.63 (t, J=7.6 Hz, 2H), 2.00-2.08 (m, 2H), 1.82-1.90 (m, 2H), 1.76-1.81 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829244B2
Source datasetuspto-grants-2014_09
ORD IDord-4a7fce714a434bd1b433e20af721d168
Source noteuspto-grants-2014_09