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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766823Generated: October 25, 2026

Triethylamine → 2-(2-Hydroxy-3,3-dimethylbutoxy)-isoindole-1,3-dione

https://huagongshe.com/reaction/1766823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-HydroxyphthalimideHCID 10665—
Reactant2-tert-ButyloxiraneHCID 92174—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(2-Hydroxy-3,3-dimethylbutoxy)-isoindole-1,3-dioneHCID 2111153314%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 3,3-dimethyl-1,2-epoxybutane (5.0 mL, 41.0 mmol) in DMF (100 mL) was added N-hydroxyphthalimide (8.03 g, 49.2 mmol) and triethylamine (6.90 mL, 49.2 mmol). The solution was heated at 75° C. for two days. The solution was cooled to room temperature, diluted with ethyl acetate and washed with water (2×), saturated potassium carbonate (3×), brine (2×), dried over Na2SO4 and concentrated to an orange solid. Purification using flash column chromatography (dichloromethane) provided the desired product as a white solid (1.50 g, 14%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230099B2
Source datasetuspto-grants-2007_06
ORD IDord-51f50cf265ce474683a9368c3598e95f
Source noteuspto-grants-2007_06