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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250862Generated: October 31, 2026

4-Chlorobenzenesulfonyl chloride → HCID 69920461, compound

https://huagongshe.com/reaction/1250862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acidHCID 69922785—
SolventDimethylformamideHCID 6228—
ProductHCID 69920461HCID 69920461—

Reaction Conditions

Temperature0 °C

Reaction Steps

200 mg of 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid were dissolved in 2 ml of DMF and cooled to 0° C. 220 mg of 4-chlorobenzenesulfonyl chloride and 270 mg of diisopropylethylamine were added and the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was cooled to −25° C. for 16 hours and then warmed to room temperature. The reaction was quenched by the addition of water, and the mixture was extracted three times with dichloromethane. The combined organic phases were dried with sodium sulfate, filtered and the solvent was removed in vacuo. The residue was chromatographed on silica gel eluting with dichloromethane/methanol/water/acetic acid (9/1/0.1/0.1). Yield 84 mg. MS (ES+): m/e=498.1 (M+H)+; 442.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340679B1
Source datasetuspto-grants-2002_01
ORD IDord-50f4375e25f64d2e8bea1670f24dbc54
Source noteuspto-grants-2002_01