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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238984Generated: October 31, 2026

Sodium Sulfate → HCID 68949069, compound

https://huagongshe.com/reaction/238984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantPyrrolidineHCID 31268—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 68952143HCID 68952143—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68949069HCID 6894906979.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

0.4 g of 3-Bromo-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide (0.94 mmol), 0.156 ml pyrrolidin (1.89 mmol), 160 mg sodium tert-butanolate ((1.66 mmol) and 540 mg sodium sulfate were dissolved in 15 ml of tetrahydrofuran and heated to 50° C. 120 mg of 2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (0.19 mmol) and 85 mg tri(dibenzylidenacetone)dipalladium(0) (0.09 mmol) were added and the reaction stirred for 4 h under reflux. After workup, the partially converted starting material was reacted again under the same reaction conditions until completion. The solvents were evaporated under reduced pressure, the residue was treated with dichloromethane and water, the organic layer was dried over magnesium sulfate, filtered, and the solvent was evaporated under reduced pressure. The crude product was purified with silica gel chromatography with dichloromethane/methanol (0-20%) as eluent using a semi-automated ISCO companion instrument, yielding 0.309 g of the purified product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642642B2
Source datasetuspto-grants-2014_02
ORD IDord-5ddddfc9f7ba4559995897ccf2bfb283
Source noteuspto-grants-2014_02