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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638218Generated: October 27, 2026

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

https://huagongshe.com/reaction/638218

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 mole) of 3-bromo-4-ethoxy-3-buten-2-one was combined with 5.53 (0.05 mole) of hydroxyacetamidine hydrochloride in 100 ml acetone to form a slurry. To the slurry at 25° C. was added 11.5 g (0.1 mole) 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, m.p. 147°-148° C. 1H-NMR(DMSO-d6)ppm(delta): 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 numberUS04560690
Source datasetuspto-grants-1985_12
ORD IDord-3f27b471bf8346c5b6954c4488b46dc9
Source noteuspto-grants-1985_12