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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant1-Bromo-4-(4-octoxyphenyl)benzeneHCID 2801787—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Octyloxybiphenyl-4'-yl boronic acidHCID 1085354473%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07118787B2
Source datasetuspto-grants-2006_10
ORD IDord-f3ac16df9fed435fac7e859d0dfe5baa
Source noteuspto-grants-2006_10