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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424315Generated: November 1, 2026

Chlorotrimethylsilane → 3-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acid

https://huagongshe.com/reaction/1424315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactantp-BoronophenylalanineHCID 53503—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4,6-Trimethylbenzoyl chlorideHCID 97038—
SolventDichloromethaneHCID 6344—
Product3-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acidHCID 57660948—

Reaction Steps

1.5 g (7.18 mmol) of 2-amino-3-(4-boronophenyl)propionic acid were suspended in 50 ml DCM and 7.4 ml (43.1 mmol) DIPEA and refluxed for 20 min together with 4.5 ml (35 mmol) TMSCl. The solution was cooled in an ice bath and a solution of 1.44 g (7.9 mmol) 2,4,6-trimethylbenzoyl chloride in 5 ml DCM were added dropwise. The reaction mixture was stirred 2 h at room temperature, diluted with 100 ml DCM and washed with 2 N aqueous HCl. During this washing some product precipitated which was collected. The organic phase was extracted with 2 N NaOH twice. Upon acidifying of the combined basic phases the product precipitated, which was collected and dried together with the first precipitate. The crude product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927534B2
Source datasetuspto-grants-2015_01
ORD IDord-0c7bef94f99d4f2da8782cb9b47e5567
Source noteuspto-grants-2015_01