HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128068Generated: October 26, 2026
Ethanol → Methyl 4-morpholinethiocarboximidate hydroiodide
https://huagongshe.com/reaction/128068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 4-Morpholinecarbothioamide | HCID 2393544 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 4-morpholinethiocarboximidate hydroiodide | HCID 16333240 | — |
Reaction Steps
A solution of 4.65 g. of 4-morpholinethiocarboxamide [W. G. Finnegan, et al., J. Org. Chem. 18, 779 (1952)] and 4.54 g. of iodomethane in 50 ml. of ethanol is allowed to stand 48 hours at room temperature, then diluted with 250 ml. of ether to give a colorless crystalline precipitate of methyl 4-morpholinethiocarboximidate hydroiodide. A solution of 5.76 g. of this product and 1.1 g. of hydrazine hydrate in ethanol is heated under reflux for about 2 hours and then treated with 2.1 g. of 9,10-anthracenedicarboxaldehyde in 200 ml. of ethanol and 2 ml. of glacial acetic acid by heating under reflux for 3.5 hours. The solution is filtered and then evaporated to give an orange solid which is recrystallized from ethanol-ether to give the title compound, m.p. 280° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04258181 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-31a320262aa54209a4f7df096b27985a |
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| Source note | uspto-grants-1981_03 |
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