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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009147Generated: October 26, 2026

Allyl iodide → tert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamate

https://huagongshe.com/reaction/1009147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
Reactanttert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamateHCID 86614133—
CatalystHCID 178418778HCID 178418778—
SolventTolueneHCID 1140—
Producttert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamateHCID 86614132—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of tert-butyl(S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamate (0.125 g, 0.6 mmol; see: Kurokawa, N.; Ohfune, Y. Tetrahedron 1993, 49, 6195) in toluene (6 mL), was added allyliodide 0.3 mL, 3 mmol) followed by silver(I) oxide (0.7 g, 3 mmol). The solution was stirred at 65° C. in a darkened hood for a period of 15 h. The mixture was then cooled to ambient temperature, filtered through Celite, washed with CH2Cl2, and conc. in vacuo. Purification on SiO2 (10-20% EtoAc/Hexanes) gave the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973047B2
Source datasetuspto-grants-2011_07
ORD IDord-26965e30555e479b843b6a6be808c428
Source noteuspto-grants-2011_07