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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668409Generated: November 2, 2026

Tetrahydrofuran → HCID 57612782, compound

https://huagongshe.com/reaction/1668409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-Bromovaleryl chlorideHCID 521173—
Reactant4-Benzyl-1,3-oxazolidin-2-oneHCID 559668—
ReactantButyllithiumHCID 178418339—
ProductHCID 57612782HCID 5761278299.7%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of S-(−)-4-benzyl-2-oxazolidinone (8.0 g, 45.1 mmol) in THF (75 mL) at −70° C., is added n-BuLi (19.8 mL, 49.6 mmol, 2.5 M in hexane) slowly. After stirring at −70° C. for 1 hour, 5-bromovaleryl chloride (11.7 g, 58.7 mmol) is added dropwise. After stirring at −70° C. for 20 minutes, the cooling bath is removed and the reaction mixture is warmed to 25° C. and stirred for 2 hours. The solution is diluted with 150 mL of ether, and washed with 2×100 mL of water. The combined organic layers is dried over Na2SO4 and concentrated. The crude product is purified by chromatography (hexane/EtOAc:85/15) to give a white solid (15.3 g, 99.7%). (NMR and MS data confirmed, U-3133-51-24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989441B2
Source datasetuspto-grants-2011_08
ORD IDord-e5e35b7802a24e7091b22f2f34bfd66f
Source noteuspto-grants-2011_08