Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852391Generated: October 31, 2026

Ethanesulfonyl chloride → HCID 67073865, compound

https://huagongshe.com/reaction/1852391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantHCID 67074413HCID 67074413—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductHCID 67073865HCID 67073865118%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.18 g 3-(3-amino-2-methylphenoxy)-5-fluoro-N-(2-fluoro-4-iodophenyl)-2-nitroaniline (2.3 mmol, 1 eq.) were dissolved in 9.6 mL pyridine, cooled to 0° C., treated with 292 μL ethyl sulfonyl chloride (3.1 mmol, 1.2 eq.) and stirred at 0° C. for 3 hours. The reaction mixture was diluted with toluene and concentrated in vacuo. The residue was partitioned between water and ethyl acetate. The aqueous layer was reextracted with ethyl acetate. The combined organic layers were dried, filtered and concentrated in vacuo to yield 1.6 g of the crude product, which was taken up in toluene and again concentrated in vacuo. The crude product was used in the subsequent transformations without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962606B2
Source datasetuspto-grants-2015_02
ORD IDord-c368f4071e464d6098f69d58be5101cc
Source noteuspto-grants-2015_02