HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358478Generated: October 30, 2026
Hydrogen Sulfide → 2-(Morpholin-4-yl)ethanethioamide
https://huagongshe.com/reaction/358478
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Morpholineacetonitrile | HCID 22055 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(Morpholin-4-yl)ethanethioamide | HCID 3847634 | — |
Reaction Steps
A reaction mixture was prepared from 203 ml. each of triethylamine and pyridine plus 63 g. of morpholinoacetonitrile. Hydrogen sulfide was bubbled through the heated, stirred reaction mixture for about 2.5 hours. Stirring was continued overnight at ambient temperature. The next day, H2S was passed through the heated, stirred reaction mixture for an additional 1.5 hours. At this point, the solvents were evaporated in vacuo and the residue triturated with ether. The ether was discarded and the residue dissolved in ethanol. Crystalline morpholinothioacetamide formed in the above reaction precipitated and was separated by filtration. Treatment of the filtrate with alcoholic hydrogen chloride yielded morpholinothioacetamide hydrochloride melting in the range 64°-80° C. See also J.A.C.S., 72, 2804 (1950).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04468399 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-a7bb75664c5245558b09f8612ee5d2ae |
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| Source note | uspto-grants-1984_08 |
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