Hydrochloric Acid → (3-Cyano-4-isobutoxyphenyl)boronic acid

HRID 1432774Notes

Reaction equation

HRID 1432774 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:11][CH:12]([CH3:14])[CH3:13])=[C:6]([CH:9]=1)[C:7]#[N:8].[B:15](OC(C)C)([O:20]C(C)C)[O:16]C(C)C.Cl>C1COCC1.C1(C)C=CC=CC=1>[C:7]([C:6]1[CH:9]=[C:2]([B:15]([OH:20])[OH:16])[CH:3]=[CH:4][C:5]=1[O:10][CH2:11][CH:12]([CH3:14])[CH3:13])#[N:8]

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 665851345-Bromo-2-isobutoxybenzonitrile

Product 1

HCID 54576546(3-Cyano-4-isobutoxyphenyl)boronic acid

Reagents, catalysts & solvents 2

HCID 1140TolueneSolventHCID 8028TetrahydrofuranSolvent

Procedure

5-Bromo-2-isobutoxybenzonitrile and triisopropyl borate were dissolved in a mixed solvent of THF and toluene and an n-butyllithium-hexane solution was added dropwise to the solution at a temperature below −60° C. After the temperature was elevated to −20° C., 1 M hydrochloric acid was added and the whole was stirred at room temperature to obtain (3-cyano-4-isobutoxyphenyl)boronic acid. F: 220.

Workup

  1. additionan n-butyllithium-hexane solution was added dropwise to the solution at a temperature below −60° C
  2. customwas elevated to −20° C.

Sources & evidence

ORD record
ord-00e28e147f9f40e49b010a59e92ea44d
Source dataset
uspto-grants-2009_11
Patent number
US07612108B2

Reaction notes

Loading…