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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814068Generated: October 27, 2026

Benzenesulfonyl chloride → 1-Bisbenzenesulfonylamino-2-iodo-4-methanesulfonylbenzene

https://huagongshe.com/reaction/1814068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-(2-iodophenyl)methanesulfonamideHCID 780001—
SolventPyridineHCID 1049—
Product1-Bisbenzenesulfonylamino-2-iodo-4-methanesulfonylbenzeneHCID 22504410197.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of the compound obtained in Example 8 (3) (2.20 g) in pyridine (7.4 ml), benzenesulfonyl chloride (1.57 g) was added and the mixture was stirred at 15 to 30° C. for 1 hour and at 60° C. for 1 hour. Further, to the mixture was added benzenesulfonyl chloride (1.57 g) and the mixture was stirred at 60° C. for 15 hours, and then poured into a saturated aqueous ammonium chloride solution. The precipitates were filtered off, washed with water and ether successively and dried under reduced pressure to obtain 4.22 g of the desired products as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875770B2
Source datasetuspto-grants-2005_04
ORD IDord-38b39059577745308285ae79c2707832
Source noteuspto-grants-2005_04