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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58836Generated: October 27, 2026

Imidazole → methyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoate

https://huagongshe.com/reaction/58836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriphenylphosphineHCID 11776—
ReactantIodide IonHCID 30165—
ReactantN-Boc-L-serine methyl esterHCID 7019177—
SolventDichloromethaneHCID 6344—
Productmethyl (2R)-2-(((tert-butoxy)carbonyl)amino)-3-iodopropanoateHCID 1090359168.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of triphenylphosphine (131 g, 0.500 mol) and imidazole (34 g, 0.50 mol) in DCM (600 mL) was cooled to 0° C. and iodide (127 g, 0.50 mol) was added in small portions over 0.5 h. The cooling bath was removed and the mixture was stirred for 0.5 h. After the mixture was re-cooled to 0° C., a solution of (S)-methyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate (73 g, 0.33 mol) in DCM (300 mL) was added dropwise. After the addition, the cooling bath was removed and the mixture was allowed to warm to ambient temperature and stirred for 1.5 h. The mixture was filtered and the filtrate was concentrated to remove most of the solvent. MTBE (400 mL) was added to the residue and the mixture was filtered to remove triphenylphosphine oxide. The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel to afford (R)-methyl 2-((tert-butoxycarbonyl)amino)-3-iodopropanoate (74.0 g, 68% yield) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-c4c62557219c49f4894c4f195aa68a46
Source noteuspto-grants-2016_09