Methyl iodide → Lithium cyclohexylisopropylamide

HRID 1763710노트

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HRID 1763710 반응식
[CH2:1]([Li:5])CCC.[CH:6]([NH:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)([CH3:8])[CH3:7].[O:16]=[C:17]1[C:23]2[CH:24]=[CH:25][C:26]([CH2:28][C:29]([O:31][CH2:32][CH3:33])=[O:30])=[CH:27][C:22]=2[CH:21]=[CH:20][C:19]2[CH:34]=[CH:35][CH:36]=[CH:37][C:18]1=2.CI>CCOCC.O.O1CCCC1>[CH:6]([N-:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)([CH3:8])[CH3:7].[Li+:5].[O:16]=[C:17]1[C:23]2[CH:24]=[CH:25][C:26]([CH:28]([CH3:1])[C:29]([O:31][CH2:32][CH3:33])=[O:30])=[CH:27][C:22]=2[CH:21]=[CH:20][C:19]2[CH:34]=[CH:35][CH:36]=[CH:37][C:18]1=2

참가 물질

9

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온도
-80 °C

실험 절차

Lithium isopropylcyclohexylamide is prepared by adding 10 mls. of 1.0 molar n-butyl lithium to a solution of 1.41 g. of isopropylcyclohexylamine in 100 ml. of dry tetrahydrofuran. To this solution, cooled to -80° C, there is added a solution of 2.94 g. of ethyl (5-oxo-5H-dibenzo[a,d]cyclohepten-2-yl)acetate (as prepared in Preparation 3 above) in 10 ml. of tetrahydrofuran. The mixture is left for 5 minutes, then 1.42 g. of methyl iodide is added. The reaction mixture is allowed to attain room temperature, then water and ether are added. The ethereal layer is washed with dilute hydrochloric acid and water, dried and evaporated to yield ethyl 2-(5-oxo-5H-dibenzo[a,d]cyclohepten-2-yl)propionate. This ethyl ester is refluxed for 12 hrs. in 5% aqueous potassium hydroxide, followed by acidification with dilute hydrochloric acid and ether extraction to afford 2-(5-oxo-5H-dibenzo[a,d]cyclohepten-2-yl)propionic acid.

후처리

  1. additionby adding 10 mls
  2. additionthere is added a solution of 2.94 g
  3. customto attain room temperature
  4. washThe ethereal layer is washed with dilute hydrochloric acid and water
  5. customdried
  6. customevaporated

출처 및 근거

ORD 기록
ord-a3032dcb4caa41a194abc90fda7f137b
출처 데이터셋
uspto-grants-1978_09
특허 번호
US04112114

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