HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211010Generated: October 31, 2026
Hydrochloric Acid → 4-(1-Benzylthio-1-methylethyl)-3-methoxycarbonyl-2-methylene-4-butanolide
https://huagongshe.com/reaction/2211010
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Dimethyl bromomethylfumarate | HCID 10466666 | — |
| Reactant | HCID 10702996 | HCID 10702996 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Benzylthio-1-methylethyl)-3-methoxycarbonyl-2-methylene-4-butanolide | HCID 15290465 | 38.2% |
Reaction Steps
To a stirred suspension of zinc dust (0.67 g) activated with hydrochloric acid in THF (15 ml), 2-benzylthio-2-methylpropionaldehyde (1.00 g) dissolved in THF (5 ml) and dimethyl 2-bromomethylfumarate (1.28 g) dissolved in THF (5 ml) were added dropwise in the order named while refluxing under nitrogen atmosphere. The mixture was refluxed for an additional 1.5 hours and saturated aqueous ammonium chloride solution was added to it. After cooling the mixture was filtered by celite. A reaction product was extracted with ethyl acetate from the filtrate. The organic layer was washed with 1N 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 0.63 g (38%) of the titled compound.
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-062d59d83d6c49d89a47c45720f4aab9 |
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| Source note | uspto-grants-1995_10 |
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