Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858970Generated: October 30, 2026

4-Fluorobenzenesulfonyl chloride → (S)-3-(4-benzyloxy-phenyl)-2-(4-fluoro-benzenesulfonylamino)-propionic acid

https://huagongshe.com/reaction/1858970

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantSodium CarbonateHCID 10340—
ReactantO-benzyl-L-tyrosineHCID 725701—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-(4-benzyloxy-phenyl)-2-(4-fluoro-benzenesulfonylamino)-propionic acidHCID 54304605—

Reaction Steps

A mixture of (S)-2-amino-3-(4-benzyloxy-phenyl)-propionic acid (2.7 g, 0.010 mol), 4-fluoro-benzene-sulfonyl chloride (2.0 g, 0.010 mol), and sodium carbonate (2.2 g, 0.020 mol) in a mixture of tetra-hydrofuran (20 mL) and water (20 mL) was stirred at room temperature for 3 days. The reaction mixture was partitioned between ethyl acetate and 1 M hydrochloric acid. The organic layer was washed with saturated sodium chloride solution, dried (MgSO4), and rotary-evaporated under reduced pressure to give an oil. The oil was chromatographed on silica gel (445 g, 230-400 mesh) eluting with dichloromethane-methanol (20:1), and the fractions containing product were rotary-evaporated to give a solid. The solid was recrystallized from toluene to give the title compound as a light yellow solid; yield 0.22 g (5%), mp=138-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153612
Source datasetuspto-grants-2000_11
ORD IDord-d58e91ba41a74a339dc54128179f9da6
Source noteuspto-grants-2000_11