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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515913Generated: October 28, 2026

3-Chloro-2-methyl-1-propene → Benzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-

https://huagongshe.com/reaction/515913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Allyl-4-methylbenzenesulfonamideHCID 297877—
SolventDimethylformamideHCID 6228—
ProductBenzenesulfonamide, 4-methyl-N-(2-methyl-2-propenyl)-N-2-propenyl-HCID 11230883—

Reaction Steps

3-Chloro-2-methylpropene (20 mL, 0.20 mol) is added over a period of 5 minutes to a suspension of 4-methyl-N-(prop-2-en-1-yl)benzene-1-sulphonamide (27.9 g, 0.13 mol) and potassium carbonate (28.1 g, 0.20 mol) in N,N-dimethylformamide (200 mL) cooled in an ice bath. After 20 minutes, the suspension is stirred at ambient temperature for 18 hours. The suspension is concentrated to dryness. The residue is taken up in ethyl acetate (250 mL) and water (110 mL). The aqueous phase is extracted with ethyl acetate (2×50 mL). The combined organic phases are washed successively with aqueous 3N HCl solution (50 mL), water (3×50 mL), aqueous 5% potassium bicarbonate solution (50 mL), and finally brine (50 mL). The organic phase is dried over Na2SO4, filtered and concentrated to obtain the expected compound in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-efaedebd5e5d405f8af9fcc59fd1874b
Source noteuspto-grants-2015_08