HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585366Generated: October 30, 2026
Cesium carbonate → 5(S)-[1(S)-(Boc-Amino)-2-[p-(2-methoxyethoxy)phenyl]ethyl]dihydrofuran-2-(3H)-one
https://huagongshe.com/reaction/1585366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| Reactant | 5(S)-[1(S)-(Boc-amino)-2-(p-hydroxyphenyl)ethyl]dihydrofuran-2-(3H)-one | HCID 53998523 | — |
| Solvent | 1,4-dioxane N,N-dimethylformamide | HCID 21712069 | — |
| Product | 5(S)-[1(S)-(Boc-Amino)-2-[p-(2-methoxyethoxy)phenyl]ethyl]dihydrofuran-2-(3H)-one | HCID 54191873 | — |
Reaction Steps
3.17 g (9.86 mmol) of 5(S)-[1(S)-(Boc-amino)-2-(p-hydroxyphenyl)ethyl]dihydrofuran-2-(3H)-one in 190 ml of DMF/dioxane, 1: 1, are treated, under an N2 atmosphere, with 6.4 g (19.7 mmol) of Cs2CO3 and 2.0 g (9.86 mmol) of 2-methoxyethyl iodide. Since HPLC indicates that uureacted 5(S)-[1(S)-(Boc-amino)-2-(p-hydroxyphenyl)ethyl]-dihydrofuran-2-(3H)-one is still present after 18 h at RT, a further 1.2 g of 2-methoxyethyl iodide are added in portions. As soon as HPLC indicates that the reaction is complete, the reaction mixture is poured onto 190 ml of ice-water, and the whole is extracted 3× with methylene chloride. The organic phases are washed with water and saline, dried with Na2SO4 and evaporated. Stirring up the residue with hexane in an ultrasonication bath affords the title compound: TLC Rf (D)=0.08; FAB-MS (M+H)+ =380.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05935976 |
|---|
| Source dataset | uspto-grants-1999_08 |
|---|
| ORD ID | ord-90c624a7c896432b8726371338997b9f |
|---|
| Source note | uspto-grants-1999_08 |
|---|