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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Iodothiophene | HCID 18921 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | N-Methoxy-N-methylpropionamide | HCID 11344007 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| Product | 1-(5-Iodothiophen-2-yl)propan-1-one | HCID 53403012 | 49% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853205B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-12f9a54c101a4badadd4b53d949fe5ea |
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| Source note | uspto-grants-2014_10 |
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