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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 6-Amino-2,3-dihydro-1lambda6-benzothiophene-1,1-dione | HCID 12285325 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Iodo-2,3-dihydro-1-benzothiophene 1,1-dioxide | HCID 58521906 | 37.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07294650B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-1e3dc291658d4db0ad27175201ce5268 |
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| Source note | uspto-grants-2007_11 |
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