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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108384Generated: October 30, 2026

Allyl bromide → 3-(2-[3-(2-Methyl-[1,3]dioxolan-2-yl)-propyl]-pent-4-enoyl)-oxazolidin-2-one

https://huagongshe.com/reaction/1108384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
Reactant3-[5-(2-Methyl-[1,3]dioxolan-2-yl)-pentanoyl]-oxazolidin-2-oneHCID 15453757—
ReactantHCID 178418261HCID 178418261—
SolventEthyl AcetateHCID 8857—
Product3-(2-[3-(2-Methyl-[1,3]dioxolan-2-yl)-propyl]-pent-4-enoyl)-oxazolidin-2-oneHCID 15453758—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-3 (6.0 g, 23.3 mmol) and THF (125 mL) at -78° C. was added LiN(TMS)2 (18.9 mL, 37.8 mmol, 1.0M in THF) dropwise over 10 minutes. After 20 minutes, allyl bromide was added. After 10 minutes, the reaction was warmed to 0° C. After 4.0 h, the reaction was diluted with EtOAc, washed with sat. NaHCO3, brine, dried (MgSO4) and concentrated. Flash chromatography (silica, 50% EtOAc/hexanes) gave 2-4 as an yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066648
Source datasetuspto-grants-2000_05
ORD IDord-6298f7af38924d8e90feda4c6451db83
Source noteuspto-grants-2000_05