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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963452Generated: October 29, 2026

Imidazole → HCID 17819417, compound

https://huagongshe.com/reaction/963452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 54083425HCID 54083425—
SolventDichloromethaneHCID 6344—
ProductHCID 17819417HCID 1781941778.6%

Reaction Steps

To a well-stirred mixture of polystyryl supported triphenyl phosphine (29.3 mmol) in dry dichloromethane (40 mL) under a nitrogen atmosphere was added iodine (7.44 g, 29.3 mmol). After ten minutes, imidazole (2.0 g, 29.3 mmol) was added followed in ten minutes by a solution of N-butoxycarbonyl-3-fluorovalinol (13.3 mmol) in dichloromethane (200 mL). The mixture was heated to reflux for two hours. The cooled mixture was filtered through Celiteo® and the filtrate was evaporated. The residue was dissolved in diethyl ether (150 ML) and this solution was washed with dilute aqueous sodium thiosulfate (1×75 mL) and water (2×75 mL). The organic layer was dried (Na2SO4), filtered through a pad of silica gel and evaporated to afford 3.46 grams of N-butoxycarbonyl-1-iodo-2-amino-3-fluoro-3-methyl-n-butane: 1H NMR (CDCl3) δ 4.72 (br d, 1H), 3.86 (br m, 1H), 3.56 (dd, 1H), 1.47 (s, 9H), 1.43 (m, 6H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763474
Source datasetuspto-grants-1998_06
ORD IDord-cfd1d341b771461082c47311911aaac5
Source noteuspto-grants-1998_06