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Water → 2,2-Dimethyl-3-phenylcyclopropanecarbonitrile

HRID 2240846
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HRID 2240846 반응식
[C:1]([C:3]1(C(O)=O)[CH:5]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)[C:4]1([CH3:13])[CH3:12])#[N:2].[Li+].[Cl-].C([O-])(O)=O.[Na+].O>CS(C)=O.[Cl-].[Na+].O>[CH3:12][C:4]1([CH3:13])[CH:5]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)[CH:3]1[C:1]#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962Water2회HCID 433294Lithium ChlorideHCID 516892Sodium BicarbonateHCID 135886061-Cyano-2,2-dimethyl-3-phenylcyclopropanecarboxylic Acid

생성물 1

HCID 134298982,2-Dimethyl-3-phenylcyclopropanecarbonitrile수율 76%

시약·촉매·용매 2

HCID 679
Dimethyl Sulfoxide
용매
HCID 57417360Sodium chloride; water용매

실험 절차

To a solution of 1-cyano-2,2-dimethyl-3-phenyl-cyclopropanecarboxylic acid (13.6 g, 63 mmol) in DMSO (125 mL) was added LiCl (10.72 g, 252 mmol) followed by NaHCO3 (7.96 g, 94.5 mmol) and water (4.55 g, 252 mmol). Gas evolution was observed, and within 30 minutes enough solids were dissolved to allow the milky mixture to stir. The reaction mixture was stirred at 170° C. for 18 hours, then cooled and poured into a mixture of water and brine (7/1, 800 mL) and extracted with ethyl ether. The combined organic extracts were dried over Na2SO4, filtered and evaporated under reduced pressure to give 7.79 g (76% yield) of 2,2-dimethyl-3-phenyl-cyclopropanecarbonitrile (3/1, cis/trans mixture).

후처리

  1. dissolutionwithin 30 minutes enough solids were dissolved
  2. stirringThe reaction mixture was stirred at 170° C. for 18 hours
  3. temperaturecooled
  4. extractionextracted with ethyl ether
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-a43ea3e5926b4203aa0f5050855d2aa3
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07723391B2

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