Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735503Generated: October 25, 2026

N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine → 2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-one

https://huagongshe.com/reaction/1735503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N-trimethyl-1,1-bis(1-methylethoxy)amineHCID 87682—
Reactant2-butyl-3,5-dihydro-4H-imidazol-4-oneHCID 10909654—
SolventDichloromethaneHCID 6344—
Product2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-oneHCID 13637557077.1%

Reaction Steps

A solution of 5.00 g (35.67 mmol) of 2-butyl-2-imidazolin-5-one and 7.02 g (39.24 mmol) of N,N-dimethylformamide diisopropyl acetal in 25 ml of methylene chloride was stirred at room temperature for 2.5 hours. Then, the solvent was removed on a Rotavapor, and the residue was treated with 40 ml of methylene chloride. The solution thus obtained was washed twice, each time with 10 ml of water, and dried (MgSO4) and concentrated on the Rotavapor. The residue was then dried in a high vacuum. 5.37 g of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one was obtained; the product had a content of greater than 90 percent, according to H-NMR: This corresponds to a yield of about 71 percent, based on the 2-butyl-2-imidazolin-5-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536841
Source datasetuspto-grants-1996_07
ORD IDord-df8d1464c1dd4fd1a820dd4c341dc047
Source noteuspto-grants-1996_07