HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211013Generated: October 31, 2026
Hydrochloric Acid → N-benzyl-4-(1-benzylthio-1-methylethyl)-2-ethylidene-4-butanelactam
https://huagongshe.com/reaction/2211013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2-bromomethylcrotonate | HCID 11019705 | — |
| Reactant | N-(2-benzylthio-2-methylpropylidene)benzylamine | HCID 19378136 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-benzyl-4-(1-benzylthio-1-methylethyl)-2-ethylidene-4-butanelactam | HCID 53674808 | 19% |
Reaction Steps
To a stirred suspension of zinc dust (0.53 g) activated with hydrochloric acid in THF (20 ml), methyl 2-bromomethylcrotonate (1.50 g) dissolved in THF (10 ml) and N-(2-benzylthio-2-methylpropylidene)benzylamine (2.00 g) dissolved in THF (10 ml) were added dropwise in the order named at about 30° C. under nitrogen atmosphere and ultrasonic irradiation. The mixture was stirred overnight at room temperature. To the mixture saturated aqueous ammonium chloride solution was added. The mixture was filtered by celite. A reaction product was extracted with ethyl acetate from the filtrate. The organic layer was washed with IN hydrochloric acid, water and then saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and concentrated in vacuo. The oily residue was purified by silica gel column chromatography to give 1.03 g (40%) of the titled compound No.7-1 and 0.48 g (19%) of the titled compound No.7-2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05461158 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-e03ea93b583047caa0a9dd1057e4706b |
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| Source note | uspto-grants-1995_10 |
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