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Diisobutylaluminumhydride → 4,5-Dibromofuran-2-carbaldehyde

HRID 271513
Notes
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Reaction equation

HRID 271513 reaction equation
[H-].C([Al+]CC(C)C)C(C)C.CON(C)[C:14]([C:16]1[O:17][C:18]([Br:22])=[C:19]([Br:21])[CH:20]=1)=[O:15]>O1CCCC1>[Br:21][C:19]1[CH:20]=[C:16]([CH:14]=[O:15])[O:17][C:18]=1[Br:22]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 21225700DiisobutylaluminumhydrideHCID 446297544,5-Dibromo-N-methoxy-N-methylfuran-2-carboxamide

Product 1

HCID 10852284,5-Dibromofuran-2-carbaldehydeYield 81%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

Diisobutylaluminum hydride (80 ml, 1M solution in toluene) was added to a solution of the product from Step 2 (20 g, 63.4 mmol) in tetrahydrofuran (160 ml) at −78° C. The mixture was stirred at −78° C. for 1.5 hours and was then quenched with a saturated aqueous solution of ammonium chloride (40 ml). The reaction was allowed to warm to room temperature, diluted with ethyl acetate and 5M hydrochloric acid (20 ml) and stirred for 30 minutes. The organic layer was separated, washed twice with water and then brine, dried and concentrated in vacuo to yield the title compound (12.9 g, 81%); 1H NMR (CDCl3) 9.52 (1H, s), 7.21 (1H, s).

Workup

  1. customwas then quenched with a saturated aqueous solution of ammonium chloride (40 ml)
  2. temperatureto warm to room temperature
  3. additiondiluted with ethyl acetate and 5M hydrochloric acid (20 ml)
  4. stirringstirred for 30 minutes
  5. customThe organic layer was separated
  6. washwashed twice with water
  7. dry with materialbrine, dried
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-db7036dbb1054244abd4b549c6e7eaf8
Source dataset
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07452906B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes