Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405460Generated: November 1, 2026

Hydrochloric Acid → Benzo[c]phenanthren-5-ylboronic acid

https://huagongshe.com/reaction/2405460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriisopropyl borateHCID 21531—
Reactant5-Bromobenzo[c]phenanthreneHCID 10662482—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductBenzo[c]phenanthren-5-ylboronic acidHCID 5962271160%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A flask was charged with 10.1 g of 5-bromobenzo[c]phenanthrene in an argon atmosphere. 400 mL of dehydrated diethyl ether was then added to the flask. After cooling the reaction solution to −40° C., 22 mL of a 1.6 M hexane solution of n-butyllithium was added to the reaction solution. The mixture was heated to 0° C., and stirred for 1 hour. After cooling the reaction solution to −60° C., a dehydrated diethyl ether (10 mL) solution of 14.4 g of triisopropyl borate was added dropwise to the reaction solution. The reaction solution was stirred for 5 hours while warming the reaction solution up to room temperature. After the addition of 100 mL of a 10% hydrochloric acid aqueous solution, the mixture was stirred for 1 hour. After removing the aqueous phase, the organic phase was washed with water and a saturated sodium chloride solution, and dried over magnesium sulfate. After removing magnesium sulfate by filtration, the organic phase was concentrated. The resulting solid was washed with hexane to obtain 5.37 g of the target benzo[c]phenanthrene-5-boronic acid (yield: 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08803420B2
Source datasetuspto-grants-2014_08
ORD IDord-25b4d3575b4940a48aed5ad581feb6c4
Source noteuspto-grants-2014_08