Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162035Generated: October 29, 2026

Acetonitrile → 7-Iodobenzofuran-5-sulfonyl chloride

https://huagongshe.com/reaction/1162035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Iodo-2,3-dihydrobenzofuran-5-sulfonyl chlorideHCID 53430932—
SolventChlorobenzeneHCID 7964—
Product7-Iodobenzofuran-5-sulfonyl chlorideHCID 5340297590%

Reaction Steps

AIBN (270 mg, 1.3 mmol) and NBS (2.5 g, 14 mmol) were added to 7-iodo-2,3-dihydro-benzofuran-5-sulfonyl chloride (4.4 g, 13 mmol; Intermediate 55) in chlorobenzene (30 mL) at 70° C. The heating was turned off one hour after the addition. Acetonitrile (30 mL) was added and the organic phase was washed with sodium sulphite in water. The organic phase was separated and the volatiles were evaporated to give 4 g (90%) of the title compound as yellow crystals. 1H NMR 270 MHz (CDCl3) δ ppm 7.07 (d, J=2.23 Hz, 1H) 7.90 (d, J=2.23 Hz, 1H) 8.29-8.37 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820675B2
Source datasetuspto-grants-2010_10
ORD IDord-65685197f9e04014aba6dfbd8b3a05a6
Source noteuspto-grants-2010_10