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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401569Generated: October 31, 2026

Trimethylsulfonium iodide → HCID 59454960, compound

https://huagongshe.com/reaction/1401569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsulfonium iodideHCID 75127—
ReactantHCID 10898858HCID 10898858—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 59454960HCID 5945496091.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907097B2
Source datasetuspto-grants-2014_12
ORD IDord-96c5827e4e18412fb3a5b0cd8e03c372
Source noteuspto-grants-2014_12