HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236703Generated: October 26, 2026
Sodium ethoxide → HCID 178457562, compound
https://huagongshe.com/reaction/236703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | N-Cyano-N'-propargyl-N"-(2-mercaptoethyl)guanidine | HCID 136182246 | — |
| Reactant | HCID 178433264 | HCID 178433264 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 178457562 | HCID 178457562 | 50% |
Reaction Steps
A solution of 0.029 g (0.16 m mole) of the product of step A, in 1 ml ethanol containing 0.42 m mole sodium ethoxide, was placed under a nitrogen atmosphere and cooled to 4° C. with stirring. After 5 minutes, 0.035 g (0.21 m mole) of solid 4-methyl-5-chloromethylimidazole was added. The mixture was stirred for 40 minutes, poured into brine (30 ml) and then extracted with chloroform (3×15 ml). After drying (Na2SO4), the solvent was removed by evaporation. The residue was purified by thin layer chromatography on silica gel plates using a methanol-chloroform (1:4) solvent system to give 0.022 g (50%) of the title compound as a syrup which crystallized on standing at room temperature. Trituration with chloroform gave the crystalline product, m.p. 147°-149° C. I.R. (nujol): 3360 (NH), 3300 (C≡CH), 2160 (C≡N), 1600 and 1585 (C=N) cm-1 ; n.m.r. (acetone D6): δ 8.53 (1H, NH), 7.68 (s, 1H), 7.00 (1H, NH), 4.13 (q, 2H, J=2.5 Hz), 3.73 (s, 2H), 3.53 (m, 2H), 2.73 (m, 3H), 2.21 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04157340 |
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| Source dataset | uspto-grants-1979_06 |
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| ORD ID | ord-7282e8213b7f45bb8c123a7e7043e4b0 |
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| Source note | uspto-grants-1979_06 |
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