HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767629Generated: November 2, 2026
Hydrochloric Acid → 4-Pivalamidophenylboronic acid
https://huagongshe.com/reaction/1767629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | N-(4-Bromophenyl)-2,2-dimethylpropanamide | HCID 520094 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Pivalamidophenylboronic acid | HCID 22324085 | — |
Reaction Steps
To a solution of 4-bromo-N-pivaloylaniline (1.56 g, 6 mmol) in dry THF (50 ml) at −78° C. was added t-BuLi (1.5 M in pentane, 13.3 ml, 20 mmol) and the yellow mixture was stirred for 1 h at −78° C. under N2. The reaction was quenched with B(OCH3)3 (1.7 ml, 15 mmol) and stirred for another 1 h at −78° C. The reaction mixture was then warmed to room temperature and hydrolysed with 0.5 M hydrochloric acid (50 ml) and extracted with EtOAc (3×80 ml), dried (Na2SO4) and concentrated to ca. 40 ml. n-Hexane (120 ml) was added slowly and the colorless crystalline product was filtered off and dried, yielding 1.26 g (95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235548B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-97947a233ef7408293cbb76516c7aed5 |
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| Source note | uspto-grants-2007_06 |
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