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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975668Generated: October 29, 2026

Ethyl Acetate → HCID 53824424, compound

https://huagongshe.com/reaction/975668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantAllyl chloroformateHCID 18052—
ReactantHCID 22870379HCID 22870379—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53824424HCID 53824424—

Reaction Steps

To a solution of (2R,4R)-4-(t-butyldimethylsilyloxy)-2-{(1-methylimidazol-2-yl)methyl}pyrrolidineformate (20.0 g) in tetrahydrofuran (300 ml) and water (200 ml) was added dropwise a solution of allyl chloroformate (7.45 ml) in THF (20 ml), adjusting pH to 9.0~9.5 with 5N-aqueous sodium hydroxide solution, at -3°~1° C. over 10 minutes. The mixture was stirred at the same temperature for 50 minutes. To the reaction mixture was added ethyl acetate (600 ml) and ice water (400 ml). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (100 ml). The combined organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo to give (2R,4R)-1-allyloxycarbonyl-4-(t-butyldimethylsilyloxy)-2-{(1-methylimidazol-2-yl) methyl}pyrrolidine (20.5 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608056
Source datasetuspto-grants-1997_03
ORD IDord-b19a0dbbf8844780a0c9f19003154258
Source noteuspto-grants-1997_03