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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253944Generated: November 1, 2026

Sulfonium → 3-Bromo-4-(oxetan-2-YL)pyridine

https://huagongshe.com/reaction/1253944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfoniumHCID 3015009—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Bromo-4-(oxiran-2-yl)pyridineHCID 86663360—
SolventDimethyl SulfoxideHCID 679—
Solventtert-ButanolHCID 6386—
Product3-Bromo-4-(oxetan-2-YL)pyridineHCID 6678702244.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

potassium tert-butoxide (561 mg, 5 mmol) was added to a solution of sulfonium salt (1100 mg, 5 mmol) in t-BuOH (20 mL) at room temperature. After 15 min, a solution of 3-Bromo-4-oxiranyl-pyridine (200 mg, obtained above) in DMSO (10 mL) was added dropwise at 50° C. The resulting mixture was stirred at 50° C. for 15 h. The reaction mixture was quenched with brine, and the resulting mixture was extracted with ethyl acetate twice. The combined extracts were dried over anhydrous Na2SO4. After filtration and concentration, the residue was purified by flash column and afforded the title compound (96 mg). ESI-MS m/z: 216.1 [M+1]+, Retention time 1.01 min; 1HNMR (CDCl3, 400.342 MHz) δ ppm 2.50-2.59 (m, 1H), 3.31-3.39 (m, 1H), 4.65-4.70 (m, 1H), 4.87-4.92 (m, 1H), 5.91 (t, J=8 Hz, 1H), 7.95 (d, J=8 Hz, 1H), 8.68 (d, J=8 Hz, 1H), 8.73 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455522B2
Source datasetuspto-grants-2013_06
ORD IDord-2793e48adcfb451190f62c7fdb672034
Source noteuspto-grants-2013_06