HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243251Generated: October 25, 2026
Hydrochloric Acid → 4-Octyloxybiphenyl-4'-yl boronic acid
https://huagongshe.com/reaction/1243251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1-Bromo-4-(4-octoxyphenyl)benzene | HCID 2801787 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Octyloxybiphenyl-4'-yl boronic acid | HCID 10853544 | 73% |
Reaction Steps
A solution of n-butylithium (50.97 cm3, 0.1274 mol, 2.5M in hexane) was added dropwise to a cooled (−78° C.) stirred solution of 4-bromo-4′-octyloxybiphenyl (40.00 g, 0.1108 mol) in THF (400 cm3). After 1 h, trimethyl borate (23.05 g, 0.2216 mol) was added dropwise to the reaction mixture maintaining a temperature of −78° C. The reaction mixture was allowed to warm to room temperature overnight. 20% hydrochloric acid (350 cm3) was added and the resultant mixture stirred for 1 h. The product was extracted into diethyl ether (3×300 cm3). The combined organic layers were washed with water (300 cm3), dried (MgSO4), filtered and the filtrate evaporated down under partially reduced pressure. The crude product was stirred with hexane for 30 minutes and filtered off to yield a white powder (26.20 g, 73%, m.pt. 134–136° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07118787B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-f3ac16df9fed435fac7e859d0dfe5baa |
|---|
| Source note | uspto-grants-2006_10 |
|---|