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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593028Generated: October 27, 2026

Potassium Iodide → 6-Iodo-2,3-dihydro-1-benzothiophene 1,1-dioxide

https://huagongshe.com/reaction/1593028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant6-Amino-2,3-dihydro-1lambda6-benzothiophene-1,1-dioneHCID 12285325—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product6-Iodo-2,3-dihydro-1-benzothiophene 1,1-dioxideHCID 5852190637.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 2,3-dihydro-1-benzothiophen-6-amine 1,1-dioxide (1.1 g) 2M hydrochloric acid (14 ml) was cooled in an ice-bath. Sodium nitrite (355 mg) in water (5 ml) was added dropwise and the mixture was stirred for 15 min before aqueous potassium iodide (830 mg) was added. The mixture was stirred overnight, before it was heated to 65° C. for 0.5 h. The mixture was cooled to 20° C. and extracted into ethyl acetate. The organic solution was washed with aqueous sodium metabisulfite solution, brine, dried and purified on two SPE silica cartridges (10 g) eluting with dichloromethane, diethyl ether and ethyl acetate. The dichloromethane fractions were combined and evaporated to give the title compound (550 mg) LCMS RT=2.65 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294650B2
Source datasetuspto-grants-2007_11
ORD IDord-1e3dc291658d4db0ad27175201ce5268
Source noteuspto-grants-2007_11