Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714564Generated: October 30, 2026

Imidazole → 1,1-dimethylethyl (4R)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-iodopentanoate

https://huagongshe.com/reaction/1714564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant1,1-Dimethylethyl (4r)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-hydroxypentanoateHCID 10108236—
SolventDichloromethaneHCID 6344—
Product1,1-dimethylethyl (4R)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-iodopentanoateHCID 5759423377%

Reaction Steps

To a solution of crude 1,1-dimethylethyl (4R)-4-({[(1,1-dimethylethyl)oxy]carbonyl}amino)-5-hydroxypentanoate (23.8 g, 82.4 mmol), triphenylphosphine (32.42 g, 123.6 mmol) and imidazole (8.41 g, 123.6 mmol) in 515 mL anhydrous CH2Cl2 under N2 at 0° C. was added iodine over 15 min portionwise. The ice bath was removed and the reaction was allowed to warm to room temperature and stirred over 30 minutes. The reaction was quenched with 200 mL H2O. The aqueous layer was extracted with diethyl ether (2×150 mL). The combined organic layers were washed with sat. aq. Na2SO3 solution (2×25 mL) and brine (25 mL), dried over MgSO4, and concentrated, in vacuo. Purification of the residue by silica gel chromatography (Analogix IF280, 5%-50% EtOAc/Hex) afforded the title compound as a white solid (25.34 g, 77%). ESMS [M+H]+=400.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795448B2
Source datasetuspto-grants-2010_09
ORD IDord-22e3970c1eb64c4594bf2e3e4ec7320f
Source noteuspto-grants-2010_09