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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760382Generated: November 2, 2026

Imidazole → (R)-tert-Butyl (2-fluoro-3-iodopropyl)carbamate

https://huagongshe.com/reaction/1760382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(R)-tert-Butyl (2-fluoro-3-hydroxypropyl)carbamateHCID 9899077—
SolventDichloromethaneHCID 6344—
Product(R)-tert-Butyl (2-fluoro-3-iodopropyl)carbamateHCID 981491768.9%

Reaction Steps

Imidazole (26.6 g, 0.39 mol) was dissolved in methylene chloride (400 mL) at room temperature. Iodine (102.5 g, 0.39 mol) was added and the reaction mixture was stirred for 10 min at room temperature and then cooled to 0° C. Triphenylphosphine (102.5 g, 0.39 mol) was added portionwise over 10 min such that the internal temperature remained below 10° C. A solution of tert-butyl (2R)-2-fluoro-3-hydroxypropylcarbamate (60.4 g, 0.31 mol) in methylene chloride (100 mL) was added dropwise. On completion of addition of tert-butyl (2R)-2-fluoro-3-hydroxypropylcarbamate, additional methylene chloride (200 mL) was added. The reaction mixture was allowed to warm to room temperature and stirring was continued for 17 h. The reaction mixture was filtered through a pad of Celite® (50 g) and washed with additional methylene chloride. The filtrate was concentrated under reduced pressure and purified by silica gel column chromatography eluting with methylene chloride. This procedure afforded tert-butyl (2R)-2-fluoro-3-iodopropylcarbamate as a white solid (64.7 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841698B2
Source datasetuspto-grants-2005_01
ORD IDord-1c13649fa389480ba5d56c7949472bfe
Source noteuspto-grants-2005_01