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N-bromobutanimide → 5-Bromo-2,2-dimethyltetrahydro-4H-pyran-4-one

HRID 541472
Notes
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Reaction equation

HRID 541472 reaction equation
[CH3:1][C:2]1([CH3:9])[CH2:7][C:6](=[O:8])[CH2:5][CH2:4][O:3]1.[Br:10]N1C(=O)CCC1=O.C([O-])(=O)C.[NH4+]>CCOCC.C(OCC)(=O)C>[Br:10][CH:5]1[CH2:4][O:3][C:2]([CH3:9])([CH3:1])[CH2:7][C:6]1=[O:8]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 67184N-bromobutanimideHCID 517165Ammonium AcetateHCID 17381592,2-Dimethyltetrahydropyran-4-one

Product 1

HCID 682890115-Bromo-2,2-dimethyltetrahydro-4H-pyran-4-oneYield 31.5%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolvent
HCID 8857
Ethyl Acetate
Solvent

Conditions

Temperature
25 °C

Procedure

Into around-bottom flask, was placed a solution of 2,2-dimethyloxan-4-one (1.00 g, 7.80 mmol, 1.00 equiv) in ether (20 mL). N-Bromosuccinimide (1.50 g, 25.5 mmol, 3.26 equiv) was added in portions, followed by the addition of ammonium acetate (60.0 mg, 0.78 mmol, 0.10 equiv). The resulting mixture was stirred overnight at 25° C., then diluted with ethyl acetate (20 mL). The resulting mixture was washed brine (2×40 mL), dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:30) as the eluent to obtain the title compound as a yellow oil (508 mg, 31%).

Workup

  1. customInto around-bottom flask, was placed
  2. washThe resulting mixture was washed brine (2×40 mL)
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:30) as the eluent

Sources & evidence

ORD record
ord-f8f003754f1b4c9e8089945a3763de34
Source dataset
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08871790B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes