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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289007Generated: October 30, 2026

Iodine → 4-Iodophenylalanine

https://huagongshe.com/reaction/2289007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantL-PhenylalanineHCID 6140—
SolventAcetic AcidHCID 176—
SolventSulfuric AcidHCID 1118—
Product4-IodophenylalanineHCID 134497132.8%

Reaction Conditions

Temperature35 °C

Reaction Steps

Into a solution of 40.15 gm (0.243 mol) of phenylalanine in a mixture of 220 mL of acetic acid and 29 mL of concentrated H2SO4 was added 24.65 gm (0.097 mol) of powered iodine and 10. 18 gm(0.051 mol) of powered NaIO3 while stirring. The reaction mixture was stirred at 70° C. for 21 h, during this time, two portions of 1 gm of NaIO3 were added. The mixture was cooled and the acetic acid was removed by using rotavapor while temperature was maintained at 35° C. and the residue oil was diluted by adding 400 mL of water. The aqueous solution was extracted once with 100 mL ether and once with 100 of dichloromethane. After decolorization with 5 gm of Norit, the aqueous solution was neutralized by adding solid NaOH to precipitate the crude product, which, after chilling, was filtered and rinsed with 800 mL of water and 300 mL of ethanol. The wet product was recrystallized from 200 mL of acetic acid to produce 37.5 gm of 4-iodo-L-phenylalanine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090933
Source datasetuspto-grants-2000_07
ORD IDord-0ea60edda59241119ff52025839c60c0
Source noteuspto-grants-2000_07