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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328360Generated: October 25, 2026

Water → 3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dione

https://huagongshe.com/reaction/328360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
Reactantalpha-Isopropyl-alpha-methyl-1,3-dioxo-2-isoindolineacetamideHCID 4916589—
SolventTolueneHCID 1140—
Product3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dioneHCID 272924781.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 130.1 g (0.5 mole) of α-isopropyl-α-methyl-1,3-dioxo-2-isoindolineacetamide in 650 ml toluene is heated with vigorous stirring under a Dean-Stark water separator in order to remove traces of water. The solution was cooled to 100° C and 2.0 g sodium hydroxide in the form of pels is added and the mixture rapidly heated to reflux. Water collects in the water separator. One-half hour after the addition of the sodium hydroxide, a further 2 g is added and heating is continued for a further 11/4 hours when no further water is removed from the reaction mixture and the infrared spectrum of an aliquot indicates the reaction to be complete. The reaction mixture is cooled to room temperature, filtered and the solids washed with toluene and the toluene removed in vacuo to leave a white solid which is transferred to a filter funnel with hexane and air-dried to give 98.7 g of 3-isopropyl-3-methyl-3H-imidazo[2,1-a]isoindole-2,5-dione, melting point 93°-96° C. The product may be purified by recrystallization from hexane to give an analytically pure sample, melting point 98°-100.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04017510
Source datasetuspto-grants-1977_04
ORD IDord-1d50c0958c4d4d41949ae4f0571ae45b
Source noteuspto-grants-1977_04