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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612757Generated: October 30, 2026

Carbon Dioxide → HCID 12079073, compound

https://huagongshe.com/reaction/612757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium BicarbonateHCID 516892—
ReactantNSC55572HCID 5356375—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 12079073HCID 1207907389.8%

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a 12 liter four necked round bottom flask with a mechanical stirrer, thermometer, addition funnel and condenser, under nitrogen, was added 700 grams of (Z)-4-(tert-butylamino)-4-oxo-2-butenoic acid (4.0 moles) and 7757 grams of dichloromethane. The mixture was cooled to -5° C. and 438.6 grams of ethyl chloroformate (4.0 moles) was added. The mixture was cooled to -10° C. and 408.9 grams of triethylamine (4.0 moles) was added slowly at a rate such that the temperature remained below -7° C. Stirring was continued at -5° C. for 2.5 hours during which time the evolution of carbon dioxide was observed. The mixture was warmed to 11° C. and a premix of 272 grams of sodium bicarbonate dissolved in 3640 grams of distilled water was added. The mixture was stirred for 10 minutes, phase split, and the aqueous phase was removed. The organic phase was extracted three times with 3 L each of distilled water. The organic phase was dried with 275 grams of sodium sulfate, filtered and the solvent was removed in vacuo at 30° C. The residue was purified by distillation (50° C., 0.05 mm Hg) to give 550 grams of 5-(tert-butylimino)-2,5-dihydro-2-furanone. This material is hereinafter referred to as tert-butylisomaleimide. 13-CNMR shows this to be greater than 99% pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005062
Source datasetuspto-grants-1999_12
ORD IDord-4a08a6cc723c4f8b9f93f19253eda701
Source noteuspto-grants-1999_12