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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522514Generated: October 25, 2026

1-Chloro-4-iodobenzene → 2-(4-Chlorophenyl)benzo[b]thiophene-3-carbaldehyde

https://huagongshe.com/reaction/522514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-iodobenzeneHCID 12510—
Reactant1-Benzothiophene-3-carbaldehydeHCID 227328—
ReactantLithium ChlorideHCID 433294—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chlorophenyl)benzo[b]thiophene-3-carbaldehydeHCID 1162319587%

Reaction Conditions

Temperature25 °C

Reaction Steps

Benzo[b]thiophene-3-carbaldehyde (27) (162 mg, 1.0 mmol) in THF (2 mL) was added to a solution of TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) at 25° C. and the reaction mixture was then stirred at this temperature for 30 min according to TP 2. Pd(dba)2 (17 mg, 3 mol %) and P(o-furyl)3 (14 mg, 6 mol %) dissolved in THF (2 mL), and mixed with 1-chloro-4-iodobenzene (310 mg, 1.3 mmol, 1.3 equiv) were then transferred via cannula to the reaction mixture. The resulting mixture was stirred for 2 h at 25° C. The reaction mixture was then quenched with a sat. aq. NH4Cl solution (20 mL), extracted with diethyl ether (3×50 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/n-pentane, 1:3) furnished compound 29b (236 mg, 87%) as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334237B2
Source datasetuspto-grants-2016_05
ORD IDord-726a5057ea6d4016b726d656ff0db3a7
Source noteuspto-grants-2016_05