Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758759Generated: November 2, 2026

1,1,3,3-Tetramethylguanidine → HCID 178467224, compound

https://huagongshe.com/reaction/1758759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant2-Hydroxy-acetamidine hydrochlorideHCID 12217366—
Reactant3-Bromo-4-ethoxybut-3-EN-2-oneHCID 53423743—
SolventAcetoneHCID 180—
ProductHCID 178467224HCID 17846722421%

Reaction Steps

9.7 g (0.05 mol) of 3-bromo-4-ethoxy-3-buten-2-one was combined with 5.53 (0.05 mol) of hydroxyacetamidine hydrochloride in 100 ml acetone to form a slurry. To the slurry at 25° was added 11.5 g (0.1 mol) of 1,1,3,3-tetramethylguanidine over a period of 5 minutes. After stirring for 48 hours the slurry was filtered and the mother liquors were concentrated in vacuo to an oil which was chromatographed on silica gel 60 (E. Merck) using chloroform as eluent to give 1.48 g (21%) of 2-hydroxymethyl-4-acetylimidazole, mp 147°-148°. nmr (DMSO-d6) (δ): 7.73 (s, 1H); 5.46 (very broad s, 1H); 4.5 (broad s, 2H); 2.4 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374843
Source datasetuspto-grants-1983_02
ORD IDord-e850f63d307542a3a6e13ce379bb570b
Source noteuspto-grants-1983_02