HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,3,3-Tetramethylguanidine → HCID 178467224, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Reactant | 2-Hydroxy-acetamidine hydrochloride | HCID 12217366 | — |
| Reactant | 3-Bromo-4-ethoxybut-3-EN-2-one | HCID 53423743 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178467224 | HCID 178467224 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04560690 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-3f27b471bf8346c5b6954c4488b46dc9 |
| Source note | uspto-grants-1985_12 |