4-Iodotoluene → Tolylboronic acid

HRID 2121737Notes

Reaction equation

HRID 2121737 reaction equation
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.C([Li])CCC.C([O:18][B:19](OCCCC)[O:20]CCCC)CCC>C(OCC)C>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([B:19]([OH:20])[OH:18])=[CH:3][CH:4]=1

Participants

5

Conditions

Temperature
0 °C

Procedure

To a solution of 4-iodotoluene (35 g, 160.5 mmol) in diethyl ether (400 mL) was added n-butyllithium (2 M in pentane, 88.3 mL, 176.6 mmol) at 0° C. After stirring at 0° C. for another 15 min the solution was cooled to −60° C. and tributylborate (60.6 mL, 224.7 mmol) was added. The cooling bath was removed and the reaction allowed to heat up to room temperature. The solution was acidified with hydrochloric acid (2 N, 280 mL) and the organic phase separated off. The aqueous phase was extracted with diethyl ether 2×125 mL). The combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL). The combined aqueous extracts were acidified to give 18.6 g of the desired material.

Workup

  1. temperaturewas cooled to −60° C.
  2. customThe cooling bath was removed
  3. temperatureto heat up to room temperature
  4. customthe organic phase separated off
  5. extractionThe aqueous phase was extracted with diethyl ether 2×125 mL)
  6. extractionThe combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL)

Sources & evidence

ORD record
ord-ed7d91627bc045baadbd39c8ad74fa2e
Source dataset
uspto-grants-2004_02
Patent number
US06696475B2

Reaction notes

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