HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411603Generated: November 1, 2026
Chlorosulfonic acid → HCID 18541162, compound
https://huagongshe.com/reaction/411603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 4-(2-phenoxyethyl)Morpholine | HCID 2840999 | — |
| Reactant | 29488-54-8 | HCID 69960699 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18541162 | HCID 18541162 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559167B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-dbb985ddc5d043828975100e1d40228c |
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| Source note | uspto-grants-2003_05 |
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