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Acetic Acid → Methyl 5-cyano-2-oxo-5-phenylcyclohexanecarboxylate

HRID 76953
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HRID 76953 반응식
COC(C(C(OC)=O)C[CH2:7][C:8]([C:18]#[N:19])([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:9]CC)=O.[CH3:24][C:25]([O-:28])(C)[CH3:26].[K+].[C:30]([OH:33])(=[O:32])C.[C:34]1(C)C=CC=CC=1>O1CCCC1>[CH3:34][O:33][C:30]([CH:24]1[CH2:9][C:8]([C:18]#[N:19])([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:7][CH2:26][C:25]1=[O:28])=[O:32]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 1140TolueneHCID 23665647Potassium tert-butoxideHCID 690114114-Cyano-4-phenyl heptane dicarboxylic acid dimethylester

생성물 1

HCID 582396Methyl 5-cyano-2-oxo-5-phenylcyclohexanecarboxylate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

4-cyano-4-phenyl heptane dicarboxylic acid dimethylester (19.8 g, 68 mmol) was dissolved in dry tetrahydrofuran (480 mL). Potassium tert-butylate (13.2 g, 120 mmol) was then added in portions. During this addition the reaction mixture changed colour to orange. The batch was then boiled for 5 h with reflux. A brown solution was formed during boiling. The reaction mixture was cooled to room temperature overnight. 2.5N acetic acid (230 mL) was slowly added in drops to the reaction mixture with ice cooling. The batch was then mixed with toluol (100 mL), the organic phase separated and washed with saturated NaHCO3 solution (3×100 mL), H2O (3×50 mL) and NaCl solution (1×100 mL). After drying with Na2SO4 the solvent was distilled off in a vacuum. A yellowish solid remained.

후처리

  1. additionDuring this addition the reaction mixture
  2. temperaturewith reflux
  3. customA brown solution was formed
  4. customthe organic phase separated
  5. washwashed with saturated NaHCO3 solution (3×100 mL), H2O (3×50 mL) and NaCl solution (1×100 mL)
  6. dry with materialAfter drying with Na2SO4 the solvent
  7. distillationwas distilled off in a vacuum

출처 및 근거

ORD 기록
ord-77c11b1555894894baf067a9c69607c1
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835689B2

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