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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Carbonate → Ethyl phenylcyanoacetate

HRID 475847
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HRID 475847 반응식
[H-].[Na+].[CH2:3]([C:10]#[N:11])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:12](=O)([O:16]CC)[O:13][CH2:14][CH3:15]>C1COCC1>[C:10]([CH:3]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:12]([O:13][CH2:14][CH3:15])=[O:16])#[N:11]
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참가 물질

5

반응물 3

HCID 7766Diethyl CarbonateHCID 8794PhenylacetonitrileHCID 24758Sodium hydride

생성물 1

HCID 95298Ethyl phenylcyanoacetate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
40 °C

실험 절차

To a solution of sodium hydride (24.5 g, 1.02 mol) in THF was added benzyl cyanide (50.0 g, 0.426 mol) at −10° C. The reaction mixture was stirred for 15 min at the same temperature. Diethyl carbonate (60.5 g, 0.512 mol) was added to the reaction mixture and the reaction mixture was allowed to come to room temperature and heated to 40° C. (Caution: Reaction will start suddenly and exothermic). The heating path was removed immediately once the reaction was started and the reaction mixture was cooled under ice/acetone. The solution was allowed to come to room temperature and stirred for 1 h. The reaction mass was cooled to 0° C. and quenched with aqueous saturated ammonium chloride and extracted with ethyl acetate (250 mL×3). The combined organic layer was washed with water (200 mL), brine solution (200 mL), dried over anhydrous Na2SO4 and evaporated under reduced pressure to give ethyl 2-cyano-2-phenylacetate as crude compound as crude compound (71.0 g). The crude compound was taken to the next step without further purification. LC-MS (M+H)+=190.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.45 (5H, m), 5.65 (1H, s), 4.18 (2H, m), 1.18 (3H, t, J=7.2 Hz).

후처리

  1. customto come to room temperature
  2. customReaction
  3. customThe heating path was removed immediately once the reaction
  4. temperaturethe reaction mixture was cooled under ice/acetone
  5. customto come to room temperature
  6. stirringstirred for 1 h
  7. temperatureThe reaction mass was cooled to 0° C.
  8. customquenched with aqueous saturated ammonium chloride
  9. extractionextracted with ethyl acetate (250 mL×3)
  10. washThe combined organic layer was washed with water (200 mL), brine solution (200 mL)
  11. dry with materialdried over anhydrous Na2SO4
  12. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-b5db2d3703ab4b08866e8690df07aef2
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637525B2

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