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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539619Generated: October 25, 2026

Imidazole → [1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/539619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphane dichlorideHCID 13797396—
ReactantTert-butyl [1-(4-fluorophenyl)-2-hydroxyethyl]carbamateHCID 58200246—
SolventDichloromethaneHCID 6344—
Product[1-(4-Fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl esterHCID 5820031458%

Reaction Steps

To a room temperature solution of triphenylphosphine dichloride (1.53 g (5.85 mmol) in methylene chloride was added iodine (1.481 g, 5.85 mmol). The mixture was stirred for fifteen minutes, then imidazole (663 mg, 9.74 mmol) was added. The mixture was stirred another 15 minutes, then [1-(4-fluoro-phenyl)-2-hydroxy-ethyl]carbamic acid tert-butyl ester (1.0 g, 3.9 mmol) was added. The mixture was heated to reflux for two hours, then stirred at room temperature overnight. Solvent was removed under reduced pressure, and the residue was partitioned between ethyl acetate and saturated aqueous sodium thiosulfate. The organic layer was separated, washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was chromatographed through silica (5-10% ethyl acetate/hexanes) to give 820 mg (58%) of [1-(4-fluoro-phenyl)-2-iodo-ethyl]-carbamic acid tert-butyl ester, MP=138-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871760B2
Source datasetuspto-grants-2014_10
ORD IDord-4d1d6fe8d4b04a86b69a86abb67c3011
Source noteuspto-grants-2014_10