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

HRID 12054
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인쇄 미리보기

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HRID 12054 반응식
[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
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참가 물질

7

반응물 4

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

생성물 1

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

시약·촉매·용매 2

HCID 83717Copper iodide촉매
HCID 8028
Tetrahydrofuran
용매

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온도
0 °C

실험 절차

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]+.

후처리

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

출처 및 근거

ORD 기록
ord-471a2517555541d38d29395f8a35a9fa
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07727979B2

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