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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386985Generated: October 25, 2026

Iodine → 2-Iodo-3-(4-methoxyphenoxy)benzo[b]thiophene

https://huagongshe.com/reaction/1386985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant3-(4-Methoxyphenoxy)benzo[b]thiopheneHCID 10824975—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Iodo-3-(4-methoxyphenoxy)benzo[b]thiopheneHCID 10691279—

Reaction Steps

A solution of 133 mg (0.52 mmol) of 3-(4-methoxyphenoxy)benzo[b]thiophene (Part A) in 3 mL of THF was treated with 0.33 mL of 1.6 M n-BuLi in hexanes (0.54 mmol) at −78° C. for 15 min and then treated with 138 mg (0.54 mmol) of I2 in 3 mL of THF. The reaction was allowed to gradually warm to room temperature and then partitioned between brine and EtOAc/hexanes. The two phases were separated, the organic phase was washed with H2O, dried over Na2SO4, and concentrated in vacuo. The residue was crystallized from hexanes to afford 143 mg (0.37 mmol; 72%) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-e24f8b5bbe76440ea6c3491bd4deaad9
Source noteuspto-grants-2001_07