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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089855Generated: November 1, 2026

L-Phenylalanine → HCID 15045083, compound

https://huagongshe.com/reaction/1089855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-PhenylalanineHCID 6140—
ReactantHCID 15045075HCID 15045075—
SolventPotassium CarbonateHCID 11430—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15045083HCID 15045083—

Reaction Steps

3-(Fluoren-9-yl)propionyl chloride (described in Example 33; without crystallization) (3.0 g, 11.7 mmol) in dioxane (40 mL) was added to a stirred solution of L-phenylalanine ((2.0 g, 11.7 mmol) in 75 mL of 10% potassium carbonate solution and 38 mL of dioxane at room temperature. The reaction mixture was stirred overnight. The dioxane was removed under reduced pressure. The residue was diluted with water (100 mL) and extracted with ethyl acetate (4×30 mL). The water solution was treated with Norit then acidified to pH 1. The precipitate was filtered off, washed with 1N HCl, water and dried. Short path chromatography (RP-18 Silica, 50% methanol/water) afforded white solid. Final purification was accomplished by washing the product with ether. The resulting yield of N-[9H-(3-fluoren-9-ylpropionyl)]-L-phenylalanine was 1.2 g 26.5%), mp 194°-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079260
Source datasetuspto-grants-1992_01
ORD IDord-10006cb8b4b44a7c8b7974f6d52b742f
Source noteuspto-grants-1992_01