Anthraquinone → HCID 22138029, compound

HRID 1827604Notes

Reaction equation

HRID 1827604 reaction equation
Br[C:2]1[CH:3]=[C:4]([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[CH2:18]([Li])[CH2:19][CH2:20][CH3:21].[CH:23]1[C:36]2[C:35](=[O:37])[C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:28](=[O:38])[C:27]=2[CH:26]=[CH:25][CH:24]=1.[Cl-].[NH4+]>CCCCCC.C1COCC1.C1(C)C=CC=CC=1>[CH:18]1[C:10]2[CH:9]=[C:8]([C:4]3[CH:3]=[C:2]([C:35]4([OH:37])[C:34]5[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=5[C:28]([C:6]5[CH:7]=[CH:2][CH:3]=[C:4]([C:8]6[C:17]7[C:12]([C:11]8[CH:3]=[CH:2][CH:7]=[CH:6][C:10]=8[CH:9]=6)=[CH:13][CH:14]=[CH:15][CH:16]=7)[CH:5]=5)([OH:38])[C:27]5[C:36]4=[CH:23][CH:24]=[CH:25][CH:26]=5)[CH:7]=[CH:6][CH:5]=3)[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]=2[CH:21]=[CH:20][CH:19]=1

Participants

8

Reactant 4

HCID 6780AnthraquinoneHCID 25517Ammonium ChlorideHCID 221380473-(1-Naphthyl)-1-bromobenzeneHCID 178418339Butyllithium

Product 1

HCID 22138029HCID 22138029, compound

Reagents, catalysts & solvents 3

HCID 1140TolueneSolventHCID 8028TetrahydrofuranSolventHCID 8058HexaneSolvent

Procedure

Under an atmosphere of argon, 1-(3-bromophenyl)naphthalene (6.5 g, 20 mmole, 2.8 eq) was dissolved into a mixed solvent composed of anhydrous toluene (25 ml) and anhydrous THF (25 ml) and the resultant solution was cooled at −25° C. in a dry ice/methanol bath. To the cooled solution, a hexane solution of n-butyllithium (1.50 mole/liter, 15 ml, 23 mmole, 1.1 eq) was added and the resultant solution was stirred at −20° C. for 1 hour. To the obtained mixture, anthraquinone (1.5 g, 7.2 mmole) was added and the resultant mixture was stirred at −20° C. for 1 hour and at the room temperature for 3 hours and left standing for one night. To the obtained reaction mixture, a saturated aqueous solution of ammonium chloride (20 ml) was added. The formed solid was separated by filtration and washed with water, methanol and acetone and a white solid (5.9 g, quant.) was obtained.

Workup

  1. waitleft
  2. waitstanding for one night
  3. customTo the obtained reaction mixture
  4. customThe formed solid was separated by filtration
  5. washwashed with water, methanol and acetone
  6. customa white solid (5.9 g, quant.) was obtained

Sources & evidence

ORD record
ord-2ad89bb81efc455d85d7d346801415b2
Source dataset
uspto-grants-2006_05
Patent number
US07053255B2

Reaction notes

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