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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398227Generated: November 1, 2026

Water → 2-(2-Thienylmethoxy)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/2398227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-HydroxyphthalimideHCID 10665—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)thiopheneHCID 69830—
SolventDimethyl SulfoxideHCID 679—
Product2-(2-Thienylmethoxy)-1H-isoindole-1,3(2H)-dioneHCID 1070640386%

Reaction Steps

Anhydrous potassium carbonate (11.04 g.) was added to a stirred suspension of N-hydroxyphthalimide (17.12 g.) in dry dimethyl sulphoxide (200 ml.). A brown colour developed, 2-Chloromethylthiophene (28.5 g.) was added dropwise and the mixture was stirred for 16 hr., during which time the colour disappeared. The suspension was poured into water (800 ml.) and cooled to 5°. The white precipitate was filtered off, and recrystallised from ethanol to give colourless needles of N-(then-2-yloxy)phthalimide (23.4 g., 83%), m.p. 129.7°-130.9° τ values (DMSO-d6) are 4.58 (CH2), 2.28, 2.68, 2.90 (thienyl protons) 2.08 (phthalimide protons)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024137
Source datasetuspto-grants-1977_05
ORD IDord-30a4b5a4a3304e598798ad2308c9373e
Source noteuspto-grants-1977_05