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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934379Generated: November 2, 2026

Phenyl isocyanate → HCID 54382464, compound

https://huagongshe.com/reaction/1934379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantTriethylamineHCID 8471—
ReactantHCID 18734916HCID 18734916—
SolventBenzeneHCID 241—
SolventNitroethaneHCID 6587—
ProductHCID 54382464HCID 54382464—

Reaction Steps

A solution of phenylisocyanate (0.93 ml) in benzene (5 ml) was added to a mixture of 1-tert-butyldimethylsilyl-4(S)-ethynyl-2-azetidinone (1.0 g) in benzene (10 ml), nitroethane (0.35 ml), and triethylamine (0.1 ml) in benzene (5 ml) at room temperature. The reaction mixture was refluxed for 8 hours, then evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with n-hexane-ethyl acetate (9:1) to give 1-tert-butyldimethylsilyl-4(S)-(3-methyl-5-isoxazolyl)-2-azetidinone (0.96 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384028B1
Source datasetuspto-grants-2002_05
ORD IDord-4b1b7613e18146ad923babdea79490c8
Source noteuspto-grants-2002_05