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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955425Generated: October 31, 2026

Allyl bromide → HCID 11002836, compound

https://huagongshe.com/reaction/1955425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-OxazolidinoneHCID 73949—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHeptane tetrahydrofuran benzeneHCID 86600160—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11002836HCID 11002836—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 5.50 g (0.017 mol) of the oxazolidinone in 40 mL of THF, cooled to -78° C., was added 17.3 mL (0.035 mol) of a 2.0M solution of lithium diisopropylamide in heptane/THF/benzene. The resulting mixture was stirred at -78° C. for 1 h and then neat allyl bromide (7.5 mL, 0.087 mol) was added to the reaction mixture. The reaction was allowed to warm to 0 degrees (ice bath) and stirred for an additional 3 h and then quenched with 5% HCl solution. The resulting mixture was extracted with ether and the combined organic layers were washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:10) to provide 5.0 g (81%) of the desired alkylated product as a colorless oil. Electrospray Mass Spec: 358.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124502
Source datasetuspto-grants-2000_09
ORD IDord-c9de873b1f9b407bafac88e0395432a7
Source noteuspto-grants-2000_09