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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41955Generated: October 29, 2026

Tetrahydrofuran → (Benzo[c][1,2,5]oxadiazol-5-yl)methoxyphthalimide

https://huagongshe.com/reaction/41955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-HydroxyphthalimideHCID 10665—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(Bromomethyl)-2,1,3-benzoxadiazoleHCID 2735587—
Product(Benzo[c][1,2,5]oxadiazol-5-yl)methoxyphthalimideHCID 6676105594%

Reaction Steps

5-(Bromomethyl)benzo[c][1,2,5]oxadiazole (0.441 g, 2.07 mmol) was added to a solution of N-hydroxyphthalimide (0.336 g, 2.06 mmol) in dry tetrahydrofuran (15 ml). N,N-Diisopropylethylamine (0.519 g, 4.02 mmol) was added and the solution was stirred at reflux under nitrogen for 23 h and cooled to room temperature. The suspension was concentrated in vacuo to a pale beige solid. This was diluted with water and filtered. The residue was washed with plenty of water and dried under vacuum to give (benzo[c][1,2,5]oxadiazol-5-yl)methoxyphthalimide (0.571 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536157B2
Source datasetuspto-grants-2013_09
ORD IDord-b1be8216ef364d1f9a71013e80cc2570
Source noteuspto-grants-2013_09