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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411603Generated: November 1, 2026

Chlorosulfonic acid → HCID 18541162, compound

https://huagongshe.com/reaction/411603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant4-(2-phenoxyethyl)MorpholineHCID 2840999—
Reactant29488-54-8HCID 69960699—
SolventDichloromethaneHCID 6344—
ProductHCID 18541162HCID 18541162—

Reaction Conditions

Temperature0 °C

Reaction Steps

[2-(Morpholin-4-yl)ethoxy]benzene-4-sulfonyl chloride was prepared using N-(2-phenoxyethyl) morpholine by similar reaction described above. For example, 7.2 g of N-(2-phenoxyethyl)morpholine HCl salt was resuspended in 20 ml of dichloromethane and 7 ml of chlorosulfonic acid was slowly introduced with cooling by ice-jacket. The reaction mixture was stirred at 0° C. for 2 hr, then, at room temperature overnight. Dichloromethane (350 ml) was added to the reaction mixture and excess chlorosulfonic acid was destroyed by adding icy water(about 100 g). Aqueous layer was adjusted to pH 8.5 by concentrated sodium carbonate solution with cooling by ice. Dichloromethane was dried over anhydrous magnesium sulfate and evaporated under reduced pressure to give 8.1 g of [2-(morpholin-4-yl)ethoxy]benzene-4-sulfonyl chloride. M.P. 48-50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559167B1
Source datasetuspto-grants-2003_05
ORD IDord-dbb985ddc5d043828975100e1d40228c
Source noteuspto-grants-2003_05