HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl borate → 5-Chloro-2-methoxyphenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 2-Bromo-4-chloroanisole | HCID 521935 | — |
| Reactant | 5-Fluoro-2-methoxyphenylboronic acid | HCID 2782673 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 5-Chloro-2-methoxyphenylboronic acid | HCID 2735751 | 77% |
Reaction Steps
This compound was prepared in a manner similar to that of 5-fluoro-2-methoxyphenylboronic acid (EXAMPLE 107) from 2-bromo-4-chloroanisole (2.00 g, 9.0 mmol, 1.0 equivuiv), n-BuLi (2.5 M in hexanes; 3.62 mL, 9.0 mmol, 1.0 equivuiv), and trimethylborate (3.0 mL, 26 mmol, 2.9 equivuiv) to afford 1.30 g (77%) of crude 5-chloro-2-methoxyphenylboronic acid as a white semi-solid. This compound was used in the next reaction with no further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448405B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-f1e65944118f4c5691429a26c687ce2d |
| Source note | uspto-grants-2002_09 |