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Dimethylformamide diethylacetal → HCID 178484332, 화합물

HRID 1931548
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HRID 1931548 반응식
[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[O:8])=[CH:5][CH:4]=1)#[N:2].C(O[CH:15](OCC)[N:16]([CH3:18])[CH3:17])C>>[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7](/[N:9]=[CH:15]/[N:16]([CH3:18])[CH3:17])=[O:8])=[CH:5][CH:4]=1)#[N:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 70913Dimethylformamide diethylacetalHCID 76427p-Cyanobenzamide

생성물 1

HCID 178484332HCID 178484332, 화합물수율 96.1%

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온도
120 °C

실험 절차

4-cyanobenzamide (327.0 mg, 2.237 mmol) and N,N-dimethylformamide diethyl acetal (0.53 ml, 3.09 mmol) were combined and heated to 120° C. A short path distillation apparatus was used to collect the ethanol that was liberated during the reaction. The reaction mixture was a dark purple solution that slowly turned lighter until it had become an amber solution. After 70 minutes, the reaction mixture solidified. The reaction mixture was cooled to room temperature and was placed under high vacuum overnight to give the title compound (432.7 mg, 2.150 mmol) as a yellow solid.

후처리

distillation
A short path distillation apparatus
  • customto collect the ethanol that
  • customwas liberated during the reaction
  • temperatureThe reaction mixture was cooled to room temperature
  • customwas placed under high vacuum overnight
  • 출처 및 근거

    ORD 기록
    ord-0f92734a7d6a4c9690d62b9518dabb0d
    출처 데이터셋
    uspto-grants-2012_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08188085B2

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