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Anthraquinone → HCID 22138025, compound

HRID 1827614
Notes
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Reaction equation

HRID 1827614 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:9]=2)=[CH:4][CH:3]=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:7]2[C:2](=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:21]=[CH:20][C:19]=1[C:8]1[CH:17]=[CH:16][C:15]([C:35]2([OH:37])[C:34]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[C:28]([C:2]3[CH:3]=[CH:4][C:5]([C:8]4[CH:9]=[CH:10][C:11]5[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=5)[CH:17]=4)=[CH:6][CH:7]=3)([OH:38])[C:27]3[C:36]2=[CH:23][CH:24]=[CH:25][CH:26]=3)=[CH:10][CH:9]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 6780AnthraquinoneHCID 25517Ammonium ChlorideHCID 54617522-(4-Bromophenyl)naphthaleneHCID 178418339Butyllithium

Product 1

HCID 22138025HCID 22138025, compoundYield 91%

Reagents, catalysts & solvents 3

HCID 1140
Toluene
Solvent
HCID 8028TetrahydrofuranSolvent
HCID 8058HexaneSolvent

Conditions

Temperature
-20 °C

Procedure

Under an atmosphere of argon, 2-(4-bromophenyl)naphthalene (5.4 g, 19 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 −40° C. in a dry ice/methanol bath. To the cooled solution, a hexane solution of n-butyllithium (1.50 mole/liter, 14 ml, 21 mmole, 1.1 eq) was added and the resultant mixture was stirred at −20° C. for 1 hour. To the resultant solution, anthraquinone (1.4 g, 6.7 mmole) was added and the obtained 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 (3.7 g, 91%) 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

Sources & evidence

ORD record
ord-19be0ab1244849a0b8868622c82b7883
Source dataset
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07053255B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes