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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethylformamide dimethyl acetal → Ethyl 3-(dimethylamino)-2-isocyanoacrylate

HRID 649884
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인쇄 미리보기

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HRID 649884 반응식
[N+:1]([CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5])#[C-:2].CO[CH:11](OC)[N:12]([CH3:14])[CH3:13]>C(O)C>[CH2:7]([O:6][C:4](=[O:5])[C:3]([N+:1]#[C-:2])=[CH:11][N:12]([CH3:14])[CH3:13])[CH3:8]
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참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 533707Ethyl isocyanoacetate

생성물 1

HCID 54355309Ethyl 3-(dimethylamino)-2-isocyanoacrylate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of ethyl isocyanoacetate (5.0 g) in ethanol (100 mL) is added N,N-dimethyl-formamide dimethyl acetal (6.5 g) dropwise with stirring over 10 minutes. The reaction is stirred for 24 hours and the ethanol is evaporated. The resulting oil is passed through magnesium silicate using 50% ethyl acetate-hexanes as the eluant. The solvents are removed and the resulting oil is crystallized from ethyl acetate-hexanes to yield light yellow needles, 3.0 g.

후처리

  1. stirringThe reaction is stirred for 24 hours
  2. customthe ethanol is evaporated
  3. customThe solvents are removed
  4. customthe resulting oil is crystallized from ethyl acetate-hexanes
  5. customto yield light yellow needles, 3.0 g

출처 및 근거

ORD 기록
ord-5dbbb5b6d6f149409e2f95da9a895b3e
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06271236B1

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