HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424315Generated: October 31, 2026
Chlorotrimethylsilane → 3-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acid
https://huagongshe.com/reaction/1424315
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | p-Boronophenylalanine | HCID 53503 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4,6-Trimethylbenzoyl chloride | HCID 97038 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Boronophenyl)-2-(2,4,6-trimethylbenzoylamino)propionic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927534B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-0c7bef94f99d4f2da8782cb9b47e5567 |
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| Source note | uspto-grants-2015_01 |
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