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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532245Generated: October 30, 2026

2-Iodothiophene → 1-(5-Iodothiophen-2-yl)propan-1-one

https://huagongshe.com/reaction/532245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodothiopheneHCID 18921—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-Methoxy-N-methylpropionamideHCID 11344007—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran heptane ethylbenzolHCID 22742125—
Product1-(5-Iodothiophen-2-yl)propan-1-oneHCID 5340301249%

Reaction Conditions

Temperature-40 °C

Reaction Steps

38.4 ml of a 2M solution of lithium diisopropylamide (8.2 g, 76.8 mmol) in THF-heptane-ethylbenzene was added to THF (50 ml) taken in a 500 three neck RB flask equipped with a nitrogen inlet. The mixture was cooled to −40° C. and then 2-iodothiophene (16.1 g, 76.8 mmol) taken in 50 ml of THF was added with vigorous stirring. After 10 minutes the mixture was warmed to −10° C. and stirred for 30 min. The reaction mixture was re-cooled to −40° C. and N-methoxy-N-methylpropionamide (9 g, 76.8 mmol) taken in 50 ml of THF was added in one portion. The reaction mixture was allowed to warm slowly to 0° C. and then the reaction was quenched with saturated 50 ml of NH4Cl solution. The contents were extracted with 3×100 ml of DCM, dried over MgSO4 and concentrated to give an oily residue. This was purified by flash chromatography to give the title compound (10 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853205B2
Source datasetuspto-grants-2014_10
ORD IDord-12f9a54c101a4badadd4b53d949fe5ea
Source noteuspto-grants-2014_10