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1,8-dibromoanthraquinone → 1,8-Dibromoanthracene

HRID 347328
Notes
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Reaction equation

HRID 347328 reaction equation
[Br:1][C:2]1[C:15]2[C:14](=O)[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][C:12]=3[Br:17])[C:7](=O)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>CO>[Br:1][C:2]1[C:15]2[C:6](=[CH:7][C:8]3[C:13]([CH:14]=2)=[C:12]([Br:17])[CH:11]=[CH:10][CH:9]=3)[CH:5]=[CH:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 40058951,8-dibromoanthraquinoneHCID 4311764Sodium borohydride

Product 1

HCID 6306831,8-Dibromoanthracene

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
0 °C

Procedure

23.6 g (65 mmol) of 1,8-dibromoanthraquinone were suspended in 250 ml of methanol. At 10° C., 9.9 g (260 mmol) of NaBH4 were added slowly and the mixture was subsequently stirred at 0° C. for 2 hours. The mixture was poured onto 800 ml of ice, stirred and filtered under reduced pressure. The solid was subsequently suspended in 400 ml of 18% strength hydrochloric acid and stirred at 70° C. for 5 hours, after which it was once again filtered off under reduced pressure, washed until neutral and dried. The solid was stirred with 14.8 g of NaBH4 in 250 ml of isopropanol at 85° C. (reflux) for 3 hours, brought to a pH of 7 by addition of dilute hydrochloric acid, filtered off with suction and washed with water. 1,8-Dibromoanthracene was obtained in a yield of 16.2 g (74% of theory).

Workup

  1. stirringstirred
  2. filtrationfiltered under reduced pressure
  3. stirringstirred at 70° C. for 5 hours
  4. filtrationafter which it was once again filtered off under reduced pressure
  5. washwashed until neutral and
  6. customdried
  7. stirringThe solid was stirred with 14.8 g of NaBH4 in 250 ml of isopropanol at 85° C.
  8. temperature(reflux) for 3 hours
  9. additionbrought to a pH of 7 by addition of dilute hydrochloric acid
  10. filtrationfiltered off with suction
  11. washwashed with water

Sources & evidence

ORD record
ord-cffde08d9a5b4d3d8bbd90c52250cfbf
Source dataset
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07173138B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes