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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250870Generated: October 31, 2026

4-Toluenesulfonyl chloride → 4-{4-[(2S)-2-tert-Butoxycarbonyl-2-(toluene-4-sulfonylamino)-ethyl]-phenoxy}-butyric acid ethyl ester

https://huagongshe.com/reaction/1250870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl (2S)-2-amino-3-(4-(3-ethoxycarbonylpropyloxy)phenyl)propionateHCID 15512208—
SolventDimethylformamideHCID 6228—
Product4-{4-[(2S)-2-tert-Butoxycarbonyl-2-(toluene-4-sulfonylamino)-ethyl]-phenoxy}-butyric acid ethyl esterHCID 69923380—

Reaction Conditions

Temperature0 °C

Reaction Steps

411 mg of 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid ethyl ester were dissolved in 10 ml of anhydrous DMF and cooled to 0° C. 191 mg of 4-toluenesulfonyl chloride and 0.34 ml of diisopropylethylamine were added and the reaction mixture was stirred at room temperature overnight. The reaction mixture was filtered and the solvents removed in vacuo. The residue was chromatographed on silica gel eluting with n-heptane/ethyl acetate (1/1). Yield 295 mg. MS (ES+): m/e=506.2 (M+H)+; 450.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340679B1
Source datasetuspto-grants-2002_01
ORD IDord-6bc302295ade406ebea770fb217434c6
Source noteuspto-grants-2002_01