Triisopropyl borate → HCID 57356028, compound

HRID 1993239Notes

Reaction equation

HRID 1993239 reaction equation
[F:1][C:2]([F:13])([F:12])[C:3]1[C:8]2[S:9][CH:10]=[CH:11][C:7]=2[CH:6]=[CH:5][CH:4]=1.[Li]CCCC.[B:19](OC(C)C)([O:24]C(C)C)[O:20]C(C)C>C1COCC1.CCCCCC>[F:13][C:2]([F:1])([F:12])[C:3]1[C:8]2[S:9][C:10]([B:19]([OH:24])[OH:20])=[CH:11][C:7]=2[CH:6]=[CH:5][CH:4]=1

Participants

6

Conditions

Temperature
-30 °C

Procedure

To a solution of 7-trifluoromethyl-benzo[b]thiophene (0.52 g, 0.0026 mol) in THF (30 mL) at −78° C. was added 2.5 M of n-BuLi in hexane (1.4 mL). The reaction was then slowly warmed up to −30° C. over 30 min. and stirred at this temperature for 10 min prior to recooling to −78° C. and treatment with triisopropyl borate (0.7255 g, 0.0038 mol). The reaction was then slowly warmed up to 0° C. then was quenched with saturated ammonium chloride and the solvent removed in vacuo. To the residue was added aqueous sodium hydroxide (10 mL, 2N solution) followed by water (30 mL) then this mixture was extracted with DCM. The aqueous solution was acidified using dilute sulfuric acid (2N solution), filtered and the residue dried in vacuo to yield 7-trifluoromethylbenzo[b]thiophen-2-boronic acid. 1H NMR (400 MHz, MeOD) δ ppm 7.55 (1 H, t, J=7.45 Hz), 7.75 (1 H, d, J=7.07 Hz), 8.02 (1 H, s) and 8.17 (1 H, d, J=7.83 Hz).

Workup

  1. customto recooling to −78° C.
  2. temperatureThe reaction was then slowly warmed up to 0° C.
  3. customthen was quenched with saturated ammonium chloride
  4. customthe solvent removed in vacuo
  5. additionTo the residue was added aqueous sodium hydroxide (10 mL, 2N solution)
  6. extractionthis mixture was extracted with DCM
  7. filtrationfiltered
  8. customthe residue dried in vacuo

Sources & evidence

ORD record
ord-9ec6267f8c764c5c8de39cd9ca7b09fb
Source dataset
uspto-grants-2010_01
Patent number
US07651687B2

Reaction notes

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