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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethyl bromomethylfumarateHCID 10466666—
ReactantHCID 10702996HCID 10702996—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
Product4-(1-Benzylthio-1-methylethyl)-3-methoxycarbonyl-2-methylene-4-butanolideHCID 1529046538.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461158
Source datasetuspto-grants-1995_10
ORD IDord-062d59d83d6c49d89a47c45720f4aab9
Source noteuspto-grants-1995_10