HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401569Generated: October 31, 2026
Trimethylsulfonium iodide → HCID 59454960, compound
https://huagongshe.com/reaction/1401569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | HCID 10898858 | HCID 10898858 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59454960 | HCID 59454960 | 91.3% |
Reaction Steps
Potassium tert-butoxide (0.098 g, 0.80 mmol) and trimethylsulfonium iodide (0.164 g, 0.8 mmol) were mixed at RT and stirred at 0° C. To this was added 2-methyl-1-(pyridin-4-yl)propan-1-one (0.100 g, 0.671 mmol) slowly. The reaction mixture was stirred at 0° C. for 15 min. and then warmed to and stirred at 70° C. for 1 h. The reaction mixture diluted with water and extracted with EtOAc (3 10 mL), organic layer dried on sodium sulfate and concentrated under vacuum to obtain 4-(2-isopropyloxiran-2-yl)pyridine (0.1 g). 1H NMR (CDCl3, freebase) δ (ppm): 8.6 (d, 2H), 7.26 (d, 2H), 3.05 (d, 1H), 2.29 (septet, 1H), 2.26 (d, 1H), 1.65 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907097B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-96c5827e4e18412fb3a5b0cd8e03c372 |
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| Source note | uspto-grants-2014_12 |
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