HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44823Generated: October 29, 2026
Trifluoroacetic acid → HCID 58405598, compound
https://huagongshe.com/reaction/44823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 58405658 | HCID 58405658 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58405598 | HCID 58405598 | — |
Reaction Steps
To a stirring mixture of 2-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)thiazole (Compound 2-BA-1) in 50 mL of acetonitrile at rt under nitrogen were added TFA (1 mL) and NIS (10.8 g). The reaction mixture was stirred at rt overnight and an additional amount of NIS (0.5 eq to 1.0 eq) was added as needed. The crude reaction mixture was slowly quenched with ˜30 mL of a saturated aqueous Na2S2O3 solution, and ˜30 mL of a saturated aqueous NaHCO3 solution. The reaction mixture was diluted with 50 mL of EtOAc, the layers were separated and the aqueous layer was extracted with EtOAc (2×50 mL). The organic layer was purified by MPLC (eluted with 0-50% EtOAc/hex) to give 2-(4-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazol-5-yl)thiazole (Compound 4-BA-1). LCMS: 408.0 m/z (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541418B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-24decef880b34dd79d7cb6a3e58b87a3 |
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| Source note | uspto-grants-2013_09 |
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