HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475791Generated: November 3, 2026
Tetrahydrofuran → 3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic Acid
https://huagongshe.com/reaction/1475791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | (3-Bromophenethoxy)(tert-butyl)dimethylsilane | HCID 11515183 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic Acid | HCID 58845136 | — |
Reaction Steps
50.0 g of [2-(3-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane was dissolved using 500 ml of anhydrous THF and 64.6 ml of a 2.7M solution of n-butyllithium in n-heptane added dropwise at −70° C. The reaction mixture was then stirred at −70° C. for 1 h. 40.2 ml of triisopropylborate was then added dropwise at −70° C. and stirring was continued for 30 minutes at −70° C. The mixture was then allowed to warm to −20° C. and 500 ml of water added. The reaction mixture was then allowed to warm to room temperature and extracted three times using 300 ml of CH2Cl2 each. The organic layer was then dried using MgSO4 and evaporated to yield 43.6 g of the title compound, used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09018383B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-a30b4bdf301c4ec38f699ae65e041a7a |
|---|
| Source note | uspto-grants-2015_04 |
|---|