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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | tert-butyl (S)-2-hydroxy-1-((S)-oxiran-2-yl)ethylcarbamate | HCID 86614133 | — |
| Catalyst | HCID 178418778 | HCID 178418778 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl (S)-2-(allyloxy)-1-((S)-oxiran-2-yl)ethylcarbamate | HCID 86614132 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973047B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-26965e30555e479b843b6a6be808c428 |
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| Source note | uspto-grants-2011_07 |
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