Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258063Generated: October 31, 2026

Hydrochloric Acid → 4-(2,5-Dichlorophenyl)sulfonylmorpholine

https://huagongshe.com/reaction/2258063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantMorpholineHCID 8083—
ReactantTriphenylphosphineHCID 11776—
Reactant2,5-Dichlorobenzenesulfonyl chlorideHCID 79401—
CatalystZincHCID 23994—
CatalystNickel DichlorideHCID 24385—
SolventEthanolHCID 702—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(2,5-Dichlorophenyl)sulfonylmorpholineHCID 730792—

Reaction Conditions

Temperature50 °C

Reaction Steps

Anhydrous nickel(II) chloride (60 mg, 0.46 mmole), triphenylphosphine (800 mg, 3.05 mmole), sodium iodide (180 mg, 1.2 mmole), and activated zinc powder (1.2 g, 18 mmole) are placed into a 25 ml flask under an inert atmosphere along with 7 ml of anhydrous N-methylpyrrolidinone (NMP). This mixture is stirred at 50° C. for about 10 minutes, leading to a deep-red coloration. A solution of 3.4 g (11.5 mole) of 2,5-dichlorobenzenesulfonylmorpholine, which is prepared by the reaction of 2,5-dichlorobenzenesulfonyl chloride with morpholine, in 8 ml of anhydrous. NMP is then added by syringe. After stirring for 60 hours, the resulting highly viscous solution is poured into 100 ml of 1 molar hydrochloric acid in ethanol to dissolve the excess zinc metal and to precipitate the polymer. This suspension is filtered and triturated with acetone to afford, after isolation and drying, solid polyparabenzenesulfonylmorpholine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05659005
Source datasetuspto-grants-1997_08
ORD IDord-f7327a79f4bd4b6f8c24e989e02cad10
Source noteuspto-grants-1997_08