2-Bromophenol → Anthracene

HRID 1828987Notes

Reaction equation

HRID 1828987 reaction equation
Br[C:2]1[C:3]2[C:8]([CH:9]=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.BrC1C=CC=CC=1O>CCOCC.CCCCCC.[Cl-].[Cl-].[Zn+2].CC(C)([P](C(C)(C)C)([Pd][P](C(C)(C)C)(C(C)(C)C)C(C)(C)C)C(C)(C)C)C>[CH:4]1[C:3]2[C:8](=[CH:9][C:10]3[C:15]([CH:2]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:7]=[CH:6][CH:5]=1

Participants

7

Conditions

Temperature
-30 °C

Procedure

A solution of 9-bromoanthracene (0.67 g, 2.6 mmol, 1.2 eq) in dry Et2O (13 mL) under N2 was cooled to −30° C. and nBuli (1.6 M in hexane, 1.6 mL, 2.6 mmol, 1.2 eq) was added dropwise. The solution was stirred for 20 min. at −30° C. followed by dropwise addition of ZnCl2 (0.50 M in THF, 5.2 mL, 2.6 mmol, 1.2 eq). The reaction was stirred and warmed to RT over 30 min. The volatiles were removed under N2 purge and the residue was redissolved in 3:1 THF/NMP (11 mL). The MOM-protected bromophenol (2.2 mmol, 1.0 eq) and Pd(PtBu3)2 (22 mg, 44 μmol, 4 mol %) were added and the reaction was heated to 100° C. for 2 h. The reaction was cooled to RT and the THF was removed. The residue was diluted with CH2Cl2, washed with 1 M HCl, and dried over Na2SO4. The crude material was purified by flash chromatography.

Workup

  1. stirringThe reaction was stirred
  2. temperaturewarmed to RT over 30 min
  3. customThe volatiles were removed under N2
  4. custompurge
  5. dissolutionthe residue was redissolved in 3:1 THF/NMP (11 mL)
  6. temperaturethe reaction was heated to 100° C. for 2 h
  7. temperatureThe reaction was cooled to RT
  8. customthe THF was removed
  9. additionThe residue was diluted with CH2Cl2
  10. washwashed with 1 M HCl
  11. dry with materialdried over Na2SO4
  12. customThe crude material was purified by flash chromatography

Sources & evidence

ORD record
ord-78aa6b9adafc40f9993b980f242715e6
Source dataset
uspto-grants-2006_06
Patent number
US07060848B2

Reaction notes

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