HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823697Generated: October 25, 2026
11-Bromo-1-undecanol → 4-(11'-Hydroxyundecyl)carboxyphenylboronic acid
https://huagongshe.com/reaction/1823697
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 11-Bromo-1-undecanol | HCID 74163 | — |
| Reactant | 4-Carboxyphenylboronic Acid | HCID 312183 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(11'-Hydroxyundecyl)carboxyphenylboronic acid | HCID 86587481 | — |
Reaction Steps
A mixture of 4-carboxyphenylboronic acid (1.0 grams), potassium hydrogen carbonate (2.01 g), 11-bromo-1-undecanol, and N,N-dimethylformamide (60 mL) was heated at 60° C. under a nitrogen atmosphere for 18 hours. After the heating period, the mixture was allowed to cool to room temperature. The mixture was then filtered and the filtrate was concentrated on a rotary evaporator. The concentrated filtrate was diluted with ethyl acetate (500 mL) and the ethyl acetate was washed successively with saturated aqueous sodium bicarbonate (3×300 mL), followed by saturated aqueous sodium chloride (300 mL). After drying over sodium sulfate, the ethyl acetate extract was concentrated on a rotary evaporator and dried under reduced pressure to afford 2.2 grams of the desired product as a light yellow viscous oil that solidified upon standing to a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07041280B2 |
|---|
| Source dataset | uspto-grants-2006_05 |
|---|
| ORD ID | ord-4bec4ee9b17b49afbfefbe02469da0e3 |
|---|
| Source note | uspto-grants-2006_05 |
|---|