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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 2-bromomethylcrotonateHCID 11019705—
ReactantN-(2-benzylthio-2-methylpropylidene)benzylamineHCID 19378136—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductN-benzyl-4-(1-benzylthio-1-methylethyl)-2-ethylidene-4-butanelactamHCID 5367480819%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461158
Source datasetuspto-grants-1995_10
ORD IDord-e03ea93b583047caa0a9dd1057e4706b
Source noteuspto-grants-1995_10