Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660653Generated: October 28, 2026

Hydrochloric Acid → 1-Benzenesulfonyl-2-vinylpyrrolidine

https://huagongshe.com/reaction/660653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant1-Benzenesulfonylpyrrolidine-2-carbaldehydeHCID 14424904—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product1-Benzenesulfonyl-2-vinylpyrrolidineHCID 68839934—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of methyl triphenylphosphonium bromide (357 mg, 1 mmol) in THF (10 mL) at −78° C. is added dropwise KHMDS (1 mmol, 2 mL of 0.5M solution). To this yellow solution is added dropwise a solution of 1-benzenesulfonylpyrrolidine-2-carbaldehyde (235 mg, 1 mmol) in THF (1 mL). The mixture is stirred at −78° C. for 2 h then is allowed to warm to RT. The mixture is poured into 1N HCl and extracted with EtOAc. The organic phase is washed with brine and dried over magnesium sulfate then the solvent removed under reduced pressure. The resulting oil is purified by flash chromatography using a gradient of 0-20% EtOAc/hexane as eluent to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-7bdd69c47f18465dbe44e7ebe1773e6f
Source noteuspto-grants-2011_12