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Trimethyl borate → HCID 90198540, compound

HRID 1748935
Notes
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Reaction equation

HRID 1748935 reaction equation
[C:1]1([C:7]2[CH:19]=[CH:18][C:10]3[S:11][C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=4[C:9]=3[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([Li])CCC.C[O:26][B:27](OC)[O:28]C>O1CCCC1>[C:1]1([C:7]2[CH:19]=[CH:18][C:10]3[S:11][C:12]4[C:17]([B:27]([OH:28])[OH:26])=[CH:16][CH:15]=[CH:14][C:13]=4[C:9]=3[CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8470Trimethyl borateHCID 135272452-Phenyldibenzo[b,d]thiopheneHCID 178418339Butyllithium

Product 1

HCID 90198540HCID 90198540, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

2-bromo-dibenzo[b,d]thiophene (10 g), phenylboronic acid (5.1 g) tetrakis(triphenylphosphine)palladium (2.2 g) and potassium carbonate (18.38 g) were refluxed in a mixture of toluene (110 mL), ethanol (20 mL) and water (90 mL) overnight. The reaction was quenched with water and the toluene layer was removed and passed through a celite column and the toluene layer was evaporated in a rotary evaporator to yield 5.2 g 2-phenyl-dibenzo[b,d]thiophene. 2-phenyldibenzo[b,d]thiophene (5.2 g) was dissolved in anhydrous tetrahydrofuran (50 mL) under nitrogen atmosphere, and the solution was then cooled to −78° C. 20.0 mL of n-butyl lithium (1.6 M solution) was added dropwise into the reaction mixture, and continuously stirred to equilibriate to room temperature. The reaction mixture was then cool to −60° C., and trimethyborate (5.67 mL) was added and the reaction was allowed to stir overnight. The reaction was then quenched with 20% aqueous hydrochloric acid, and extracted the organic layer with ethyl acetate; ethyl acetate layer was then washed thoroughly with water and dried over anhydrous sodium sulfate, and was evaporated to dryness to yield 4.2 g of 8-phenyldibenzo[b,d]thiophene-4-boronic acid.

Workup

  1. customto equilibriate to room temperature
  2. temperatureThe reaction mixture was then cool to −60° C.
  3. stirringto stir overnight
  4. customThe reaction was then quenched with 20% aqueous hydrochloric acid
  5. extractionextracted the organic layer with ethyl acetate
  6. washethyl acetate layer was then washed thoroughly with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. customwas evaporated to dryness

Sources & evidence

ORD record
ord-8c4d668435204bb89871565690e9aebe
Source dataset
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09153787B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes