HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395244Generated: November 1, 2026
Hydrochloric Acid → B-(4-Nonylphenyl)boronic acid
https://huagongshe.com/reaction/395244
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Bromo-4-nonylbenzene | HCID 12603095 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | B-(4-Nonylphenyl)boronic acid | HCID 4589192 | 79% |
Reaction Steps
A solution of the Grignard compound prepared from 0.55 mol of magnesium and 0.37 mol of 1 -bromo-4-nonylbenzene in 550 ml of dry tetrahydrofuran is added dropwise to a solution of 0.4 mol of trimethyl borate in 400 ml of dry tetrahydrofuran at 0° C. under a protective gas atmosphere. The mixture is stirred for an additional 2.5 h at this temperature. Then 600 ml of 10% stength hydrochloric acid are added and the resulting mixture is stirred at room temperature for 30 min. After addition of 120 g of sodium chloride, the reaction mixture is extracted with tert-butyl methyl ether, the combined organic extracts are washed with saturated sodium chloride solution and dried with magnesium sulfate. The solvent is removed under reduced pressure and the raw product is recrystallized from acetonitrile, giving 72 g (79%) of 4-nonylphenylboronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06605323B1 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-4c53473a7d4441e69c036af7060e23f2 |
|---|
| Source note | uspto-grants-2003_08 |
|---|