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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274125Generated: October 27, 2026

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

https://huagongshe.com/reaction/2274125

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

Under the atmosphere of argon, 10.1 g of 5-bromobenzo[c]phenanthrene was placed in a flask, and 400 mL of dehydrated ether was added. The reaction solution was cooled to −40° C., and 22 mL of a hexane solution of 1.6 M n-butyl lithium was added. The resultant was heated to 0° C., and stirred for 1 hour. The reaction solution was cooled to −60° C., and 10 mL of a dehydrated ether solution of 14.4 g of triisopropyl borate was added dropwise. While heating the reaction solution to room temperature, stirring was continued for 5 hours. 10 mL of a 10% aqueous hydrochloric acid solution was added, followed by stirring for 1 hour. An aqueous phase was removed, and an organic phase was washed with water and saturated saline, and dried with magnesium sulfate. After filtering off magnesium sulfate, the organic phase was concentrated. The resulting solids were washed with hexane, whereby 5.37 g (yield 60%) of benzo[c]phenanthrene-5-boronic acid as an intended product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126943B2
Source datasetuspto-grants-2015_09
ORD IDord-6c9d4a7992234e29aacd9655ff030bf1
Source noteuspto-grants-2015_09