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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724882Generated: November 2, 2026

HCID 53395073, compound → HCID 53414540, compound

https://huagongshe.com/reaction/1724882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53395073HCID 53395073—
CatalystTetrabutylphosphonium chlorideHCID 75311—
CatalystHCID 178418778HCID 178418778—
SolventDiethyl EtherHCID 3283—
ProductHCID 53414540HCID 53414540—

Reaction Steps

3-{5-(4-Fluorophenyl)-2-[(4-fluorophenylamino)-(4-trimethylsilanyloxy-phenyl)methyl]-5-trimethylsilanyloxypentanoyl}-4-phenyloxazolidin-2-one (10 mg) is suspended in MTB ether (1 ml) under argon while cooling in ice. N,O-Bistrimethylsilylacteamide (20.75 μl) is added, followed by tetrabutylphosphonium chloride (4.2 mg) and silver(I) oxide (3.2 mg). The mixture is stirred at room temperature. A reaction to give 1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-trimethylsilanyloxypropyl]-4-(4-trimethylsilanyloxyphenyl)azetidin-2-one is found by means of thin-layer chromatography and LC/MS comparison (M+H,-TMS,-HOTMS: 392).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488818B2
Source datasetuspto-grants-2009_02
ORD IDord-c0347651bf6f4d7b9f4e90274e2cb860
Source noteuspto-grants-2009_02