HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropyl borate → 4-Diethylamino-3-ethylphenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | (4-Bromo-2-ethylphenyl)diethylamine | HCID 66672004 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-Diethylamino-3-ethylphenylboronic acid | HCID 66671780 | 35% |
Reaction Steps
In a manner similar to that of Example 1c, by reacting 3 g of (4-bromo-2-ethylphenyl)diethylamine (11.7 mmol) with 5.2 mL of a 2.5 M solution of n-butyllithium and 3.2 mL (14 mmol) of triisopropyl borate, 0.9 g of 4-diethylamino-3-ethylphenylboronic acid (yield=35%) is obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807708B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-1cec8ec649624f5cbc26d3dcee92cadc |
| Source note | uspto-grants-2010_10 |