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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709511Generated: October 31, 2026

Isopropanol → HCID 86696603, compound

https://huagongshe.com/reaction/709511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantMaleic AnhydrideHCID 7923—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantAzane;hydrateHCID 12896473—
SolventEthyl AcetateHCID 8857—
ProductHCID 86696603HCID 8669660316.1%

Reaction Steps

196 g (2.00 mol) of maleic anhydride was dissolved in 123 g (2.05 mol) of 2-propanol and 800 mL of ethyl acetate. Thereafter, 300 mL (2.15 mol) of triethylamine was added dropwise to the solution at an internal temperature of 10° C. or lower over 1.5 hours, and the obtained mixture was then stirred for 1 hour. Thereafter, 193 mL (2.03 mol) of ethyl chloroformate was added dropwise to the reaction mixture at an internal temperature of −5° C. or lower over 2 hours. After the mixture had been stirred for 30 minutes, the obtained reaction mixture was added dropwise to an aqueous solution containing 300 mL (2.16 mol) of 28% ammonia water and 250 g of ice. The obtained reaction mixture was left at room temperature overnight. Thereafter, 400 mL of ethyl acetate was added to reaction product, followed by stirring. Thereafter a liquid separation operation was performed on the reaction solution, so as to remove an aqueous layer. This operation was repeated three times. The obtained organic layers were gathered and were then concentrated. Recrystallized from hexane/ethyl acetate was performed, so as to obtain 50.5 g of isopropyl-(Z)-4-amino-4-oxo-2-butenoate in the form of a white solid. Yield: 16.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181203B2
Source datasetuspto-grants-2015_11
ORD IDord-e9b32101157f48789df965ef047db822
Source noteuspto-grants-2015_11