HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154915Generated: October 31, 2026
Benzyl acetate → N-(t-butyldimethylsilyl)-3-azido-4-(3-benzyloxycarbonyl 2-hydroxypropyl)-azetidin-2-one
https://huagongshe.com/reaction/1154915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl acetate | HCID 8785 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | N-(t-butyldimethylsilyl)-3-azido-4-(2-oxoethyl)azetidin-2-one | HCID 20563653 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(t-butyldimethylsilyl)-3-azido-4-(3-benzyloxycarbonyl 2-hydroxypropyl)-azetidin-2-one | HCID 20563667 | — |
Reaction Steps
A solution of benzyl acetate (0.011 mol) in anhydrous tetrahydrofuran (5 ml) is added dropwise to solution of lithium diisopropylamide (0.011 mol) in anhydrous tetrahydrofuran (20 ml) at -78° C. After stirring 15 more min at -78° C. the reaction mixture is treated dropwise with a solution of N-(t-butyldimethylsilyl)-3-azido-4-(2-oxoethyl)-azetidin-2-one (0.01 mol) in tetrahydrofuran (10 ml). The mixture is stirred at -78° an additional 15 min and then quenched with 2.5 N hydrochloric acid (10 ml). The mixture is diluted with ethyl acetate, washed with water, 5% sodium bicarbonate solution, and brine, dried with magnesium sulfate, and evaporated under vacuum to afford N-(t-butyldimethylsilyl)-3-azido-4-(3-benzyloxycarbonyl 2-hydroxypropyl)-azetidin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04298741 |
|---|
| Source dataset | uspto-grants-1981_11 |
|---|
| ORD ID | ord-9b44d0b96c4845fd9bec6323e0ba3501 |
|---|
| Source note | uspto-grants-1981_11 |
|---|