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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280758Generated: October 27, 2026

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

https://huagongshe.com/reaction/280758

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 numberUS04590299
Source datasetuspto-grants-1986_05
ORD IDord-2747fa57a1464a6f9a44d4a70ab15f94
Source noteuspto-grants-1986_05