Acetone → HCID 13866078, compound

HRID 1376535Notes

Reaction equation

HRID 1376535 reaction equation
[Br:1][C:2]1[CH2:6][C:5]([C:12](OCC)=[O:13])([C:7](OCC)=[O:8])[CH2:4][C:3]=1[Br:17].[H-].C([Al+]CC(C)C)C(C)C.CC(C)=O.[OH-].[Na+]>C1COCC1.O>[Br:1][C:2]1[CH2:6][C:5]([CH2:7][OH:8])([CH2:12][OH:13])[CH2:4][C:3]=1[Br:17]

Participants

7

Reactant 4

HCID 180AcetoneHCID 14798Sodium HydroxideHCID 138660771,2,-Dibromo-4,4-di(carboethoxy)cyclopenteneHCID 21225700Diisobutylaluminumhydride

Product 1

HCID 13866078HCID 13866078, compoundYield 85%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

Under nitrogen, a stirred solution of 8.7 g (23.5 mmol) of 1,2-dibromo-4,4-di(carboethoxy)cyclopentene (Step 4) in 70 mL of anhydrous THF at -78° C. was treated with 80 mL of diisobutylaluminum hydride (1.5M in toluene) over a 20 minute period. The reaction was allowed to warm to ambient temperature overnight and was slowly treated with 20 mL of acetone followed by 10 mL of 2.5N sodium hydroxide. Water (100 mL) was added and the solution extracted 5 times with ethyl acetate. The combined extracts were washed with brine, dried (Na2SO4), and concentrated in vacuo to give 5.7 g (85%) of 1,2-dibromo-4,4-di(hydroxymethyl)cyclopentene (10 in Synthetic Scheme III) as a colorless oil: NMR (CDCl3) δ 2.20 (s, 2H), 2.50 (s, 4H), 3.70 (s, 4H).

Workup

  1. extractionthe solution extracted 5 times with ethyl acetate
  2. washThe combined extracts were washed with brine
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-fd04c1b627c84e91a96c756008b38fd9
Source dataset
uspto-grants-1997_09
Patent number
US05663180

Reaction notes

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