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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030262Generated: November 1, 2026

Methanesulfonyl chloride → HCID 15675894, compound

https://huagongshe.com/reaction/1030262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(allyloxy)anilineHCID 6504204—
SolventPyridineHCID 1049—
ProductHCID 15675894HCID 15675894—

Reaction Steps

Methanesulfonyl chloride (5.06 mL, 65.32 mmol) was added to a stirred solution of 3-[(4-amino)phenoxy]-1-propene (8.11 g, 54.43 mmol) in pyridine (80 mL) at 0° C. The mixture was stirred for 72 hours and was then poured slowly into ice-water and extracted with ether. The organic phase was washed with cold 1N HCl and was then extracted with 1N NaOH solution. The aqueous phase was acidified and the product (9.05 g, 73%) precipitated out as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05104892
Source datasetuspto-grants-1992_04
ORD IDord-200b04e0096d49d2879b06b35f79a386
Source noteuspto-grants-1992_04