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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52189Generated: October 29, 2026

2-Iodo-3-(4fluorophenylmethyl)thiophene → 2-Methyl-3-(4-fluorophenylmethyl)thiophene

https://huagongshe.com/reaction/52189

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodo-3-(4fluorophenylmethyl)thiopheneHCID 19963279—
ReactantHCID 178418573HCID 178418573—
CatalystHCID 178418745HCID 178418745—
SolventDiethyl EtherHCID 3283—
Product2-Methyl-3-(4-fluorophenylmethyl)thiopheneHCID 1996327048%

Reaction Steps

The 2-iodo-3-(4-fluorophenylmethyl)thiophene prepared in step 1 was taken up in ether and methylmagnesium bromide (3.0M in ether, 2.42 mL, 7.26 mmol) and dichloro [1,3-bis(diphenylphosphino)propane]nickel(II) (164 mg, 0.302 mmol) were added and the reaction mixture was stirred for 17 hours at ambient temperature. The reaction mixture was quenched with saturated aqueous NH4Cl and extracted with ethyl acetate. The organic phase was washed with 1N aqueous H3PO4, saturated aqueous NaHCO3, saturated aqueous Na2S2O3, and brine, dried over MgSO4, filtered, and concentrated in vacuo. Chromatography on silica gel (10% ethyl acetate/hexane) gave 2-methyl-3-(4-fluorophenylmethyl)thiophene (602 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616596
Source datasetuspto-grants-1997_04
ORD IDord-b9357db81ccf486c92cf642395755be2
Source noteuspto-grants-1997_04