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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175637Generated: November 1, 2026

Iodine → 1-Chloro-7-iodoisoquinoline

https://huagongshe.com/reaction/2175637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant7-Bromo-1-ChloroisoquinolineHCID 6502024—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-7-iodoisoquinolineHCID 44156309—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Into a 50 mL round-bottom flask, was placed 7-bromo-1-chloroisoquinoline (as prepared in the previous step, 520 mg, 2.15 mmol, 1.00 equiv) and tetrahydrofuran (10 mL). This was followed by the addition of n-BuLi (0.85 mL, 1.25 equiv) dropwise with stirring at −78° C. in 2 min. The resulting solution was allowed to react, with stirring, for an additional 40 min at −80° C. To this was added a solution of I2 (541 mg, 2.14 mmol, 1.25 equiv) in tetrahydrofuran (3 mL) dropwise with stirring at −78° C. in 1 min. The reaction mixture was allowed to react, with stirring, overnight at 25° C. The reaction was then quenched by the addition of 1 mL of water.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062048B2
Source datasetuspto-grants-2015_06
ORD IDord-cd1b00a85c1043379ef26916ce6290be
Source noteuspto-grants-2015_06