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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289309Generated: October 31, 2026

Triisopropyl borate → (5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acid

https://huagongshe.com/reaction/1289309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
Reactant6-Bromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 10586063—
ReactantButyllithiumHCID 178418339—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
Product(5,6,7,8-Tetrahydro-5,5-dimethylnaphth-2-yl)boronic acidHCID 22571498—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cold (-78° C.) solution of 2.02 g (8.4 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene in 11.0 mL of toluene, was added 4.6 g (6.8 mL, 10.9 mmol, 1.6M in hexane) of n-BuLi. The resulting solution was stirred at -78° C. for 45 min. and then 2.40 g (3.0 mL, 12.7 mmol) of triisopropylborate was dropwise added and the reaction stirred at room temperature for 12 h. The reaction was then diluted with 10% HCl, and extracted with ether (2 x). The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give an oil. Recrystallization from hexane afforded the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747542
Source datasetuspto-grants-1998_05
ORD IDord-e1ec370d0a684745a94eba6d8640f4a3
Source noteuspto-grants-1998_05