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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663105Generated: October 31, 2026

N-Hydroxyphthalimide → HCID 67132105, compound

https://huagongshe.com/reaction/1663105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4-Pentyloxybenzyl alcoholHCID 250107—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67132105HCID 67132105—

Reaction Steps

To a stirred solution N-hydroxyphthalimide (2.45 g), 4-pentyloxybenzyl alcohol (Aldrich, 2.92 g) and triphenylphosphine (4.72 g) in THF was added drop-wise diethyl azodicarboxylate (1.2 eq.). The reaction mixture was stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure and the residue was subjected to column chromatography on silica gel (petroleum ether/EtOAc, 1/2, v/v) and gave 2-(4-pentyloxy-benzyloxy)-isoindole-1,3-dione. This phthalimide intermediate (4.35 g) was dissolved in dichloromethane and methyl-hydrazine (1.1 eq.) was added. The reaction mixture stirred at room temperature for 60 minutes and the formed solid material was removed by filtration. The filtrate was evaporated under reduced pressure and the residue was subjected to column chromatography on silica gel (petroleum ether/EtOAc, 5/1, v/v), and gave the title compound (2.55 g). 13C-NMR (CDCl3) δ 159.1, 130.1, 129.2, 114.5, 77.7, 68.0, 29.0, 28.2, 22.5, 14.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034811B2
Source datasetuspto-grants-2011_10
ORD IDord-bb8a4ab04f654109b3d72db03cd387d8
Source noteuspto-grants-2011_10