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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283383Generated: October 30, 2026

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

https://huagongshe.com/reaction/1283383

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, 2.69, 2.90 (thienyl protons) 2.08 (phthalimide protons)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975376
Source datasetuspto-grants-1976_08
ORD IDord-2808d9848db3437ba117019a1c5aee0a
Source noteuspto-grants-1976_08