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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280745Generated: October 27, 2026

Triethylamine → HCID 178467223, compound

https://huagongshe.com/reaction/280745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantHCID 54475692HCID 54475692—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178467223HCID 178467223230%

Reaction Steps

6.3 g (35 mmol) of 3-bromo-4-methoxy-3-buten-2-one, 16.7 g acetamidine hydrochloride (175 mmol) and 29.2 ml triethylamine (210 mmol) were combined in 300 ml tetrahydrofuran and heated at reflux for 6 hours. The solvent was removed in vacuo to a crude orange solid. The crude solid was dissolved in 200 ml ethyl acetate and concentrated to 25 ml by boiling off the solvent. Cooling in ice resulted in crystallization of a yellow solid. This was collected by filtration, washed first with ethyl acetate, then with ether and dried at 25° in vacuo to give 9.995 g (23%) of 1-(2-methyl-4-imidazolyl)ethanone, mp 124°-7°. nmr (DMSO-d6) (δ): 4.61 (s, 1H); 1.41 (s, 3H); 1.39 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590299
Source datasetuspto-grants-1986_05
ORD IDord-a42a9f2f867e488b95034ac7eb1b3626
Source noteuspto-grants-1986_05