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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698511Generated: October 29, 2026

Ethyl Acetate → 2-Methyl-N-{1-[4-(propylsulphonyl)phenyl]prop-2-en-1-yl}propane-2-sulphinamide

https://huagongshe.com/reaction/1698511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 87333909HCID 87333909—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Methyl-N-{1-[4-(propylsulphonyl)phenyl]prop-2-en-1-yl}propane-2-sulphinamideHCID 6727573945%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Vinylmagnesium bromide (3.3 mL of a 1.0 M solution in THF, 3.3 mmol) was added dropwise to a solution of 2-methyl-N-{(1E)-[4-(propylsulphonyl)phenyl]methylene}-propane-2-sulphinamide (1.0 g, 3.17 mmol, prepared as described in Example 50a in THF (15 mL) at −78° C. The mixture was stirred at −78° C. for 6 h and then allowed to warm to room temperature overnight. The reaction mixture was quenched by addition of saturated NH4Cl(aq) and the product extracted into ethyl acetate (×2). The combined organic extracts were dried (MgSO4) and concentrated. The product was purified by gradient chromatography on silica eluting with 30 to 80% ethyl acetate in hexane giving the title compound as a yellow solid (485 mg, 45% yield). m/z (ES+) 366 (M+Na), 344 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163956B2
Source datasetuspto-grants-2012_04
ORD IDord-2e124de7cab8495c95de7fdbe46f2cab
Source noteuspto-grants-2012_04