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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239711Generated: October 25, 2026

Propane sultone → 4-iodo-N-(3-sulfopropyl)-L-phenylalanine amide

https://huagongshe.com/reaction/239711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropane sultoneHCID 14264—
Reactant(S)-2-Amino-3-(4-iodophenyl)propanamideHCID 447705—
CatalystDimethylformamideHCID 6228—
SolventMethyl Ethyl KetoneHCID 6569—
Product4-iodo-N-(3-sulfopropyl)-L-phenylalanine amideHCID 13172700217.6%

Reaction Steps

The solid (1.96 g, 5.8 mmol) was dissolved in a minimum amount of water. To the solution was added aqueous NH4OH (28-30%, 15 mL). The reaction mixture was stirred at room temperature over weekend. The solvent was removed under reduced pressure and EtOAc (15 mL) was added. The mixture was heated under reflux. The hot solution was filtered. The filtrate was cooled to room temperature and was stored in the fridge. The solid was collected by filtration, washed with EtOAc, to give 4-iodophenylalanine amide. The amide (1.3 g, 4.4 mmol) was dissolved in 15 mL of 2-butanone with a few drops of DMF before 1,3-propane sultone (560 mg, 4.9 mmol) was added. The reaction mixture was stirred at reflux for 2 hours. The mixture was cooled to room temperature. The solid was collected by filtration, washed with acetone (2×20 mL) and dried in vacuo. The solid was suspended in MeOH (25 mL) and a small amount of water (1 mL). The suspension was stirred at reflux. The solid material was collected by filtration while the mixture was still hot. The solid was washed with hot MeOH (2×10 mL). Compound CO was obtained as a white solid (320 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642801B2
Source datasetuspto-grants-2014_02
ORD IDord-6df520c0691f42bc9e253fc46eeb4155
Source noteuspto-grants-2014_02