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Ammonium Chloride → 3,3-Dimethyl-4-phenyl-cyclohexanone

HRID 12054
Notes
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Reaction equation

HRID 12054 reaction equation
[Cl-].[Li+].[CH3:3][C:4]1[CH:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:8][CH2:7][C:6](=[O:16])[CH:5]=1.[CH3:17][Mg]Br.[Cl-].[NH4+]>O1CCCC1.[Cu](I)I>[CH3:3][C:4]1([CH3:17])[CH:9]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:8][CH2:7][C:6](=[O:16])[CH2:5]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 25517Ammonium ChlorideHCID 2383403-Methyl-4-phenylcyclohex-2-en-1-oneHCID 433294Lithium ChlorideHCID 178418573HCID 178418573, compound

Product 1

HCID 450968233,3-Dimethyl-4-phenyl-cyclohexanone

Reagents, catalysts & solvents 2

HCID 83717
Copper iodide
Catalyst
HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

Lithium chloride (0.6 mmol) and copper iodide (0.3 mmol) are introduced first under argon in dry tetrahydrofuran (18 ml). At 0° C. 3-methyl-4-phenylcyclohex-2-enone (3 mmol) is added and stirring continues for another 10 min at this temperature. Then a solution of methylmagnesium bromide (3.6 mmol) is slowly added dropwise and the reaction mixture is maintained at 0° C. for 3 hours accompanied by stirring. The reaction is stopped by adding saturated aqueous ammonium chloride solution. The mixture is extracted with diethyl ether. The title compound is obtained from the combined organic phases after drying over sodium sulphate and evaporating-off of the solvent in a vacuum (J. Organom. Chem. 1995, 502, C5-C7): tR 2.36 min (LC-2); ESI-MS (+): m/z 203.35 [M+H]+.

Workup

  1. customAt 0° C
  2. stirringby stirring
  3. extractionThe mixture is extracted with diethyl ether

Sources & evidence

ORD record
ord-471a2517555541d38d29395f8a35a9fa
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07727979B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes