HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584540Generated: October 31, 2026
N-(2-aminoethyl)acetamide → HCID 19593902, compound
https://huagongshe.com/reaction/1584540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(2-aminoethyl)acetamide | HCID 66082 | — |
| Reactant | HCID 54516579 | HCID 54516579 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19593902 | HCID 19593902 | — |
Reaction Steps
Methyl [3-(tetrahydropyran-2-ylthio)propyl]thioacetate (1 g, 3.7 mmol) was added dropwise to N-(2-aminoethyl)-acetamide (1.25 g, 12.25 mmol) and the mixture heated at 75° C. for 2.5 h. Volatile components were then removed under reduced pressure (45° C. at 0.02 mmHg) to give an oil which was taken up into water. This aqueous solution was then extracted with dichloromethane (adding potassium chloride to the aqueous layer to prevent emulsion formation if necessary). The dichloromethane extracts were then dried (MgSO4), filtered, and the solvent removed under reduced pressure to give the crude N-(2-acetylaminoethyl)-3-(tetrahydropyran-2-ylthio)propylthioacetamide. A pure sample of this material (0.25 g, 22%) was obtained by reverse phase h.p.l.c. using aqueous methanol as the eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932707 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-a33e79a7d40646a5a7631f873c5a1242 |
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| Source note | uspto-grants-1999_08 |
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