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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080415Generated: October 26, 2026

Iodine → 5-(4-Fluorophenyl)-2-iodothiophene

https://huagongshe.com/reaction/1080415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant2-[(4-Fluorophenyl)methyl]thiopheneHCID 10583905—
Reactant2-(4-Fluorobenzyl)-5-iodothiopheneHCID 10615467—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product5-(4-Fluorophenyl)-2-iodothiopheneHCID 23367310—

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 2-(4-fluorobenzyl)thiophene (8.4 g, 43.7 mmol), HIO3 (1.86 g, 10.6 mmol), I2 (4.86 g, 19.2 mmol), ethyl acetate (66 ml), acetic acid (7.7 ml) and conc. H2SO4 (0.79 ml) was heated at 35° C. overnight (GC-MS showed that all the starting material is converted to 5-(4-fluorobenzyl)-2-iodothiophene). To the reaction mixture was added brine solution (33 ml), the organic layer was separated and washed with sodium hydroxide/sodium thiosulfate solution (33 ml) (prepared from 2.3 g of NaOH, 3.3 g of Na2S2O3 in 27 ml of H2O), followed by 10% of NaHCO3 solution (33 ml). The organic layer was concentrated to yield 13.9 g of 5-(4-fluorophenyl)-2-iodothiophene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580989
Source datasetuspto-grants-1996_12
ORD IDord-ba49f26fae5847c386a7b6e0ba744788
Source noteuspto-grants-1996_12