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4-Hydroxybenzaldehyde → N-[(4-Hydroxyphenyl)methyl]formamide

HRID 2371091
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HRID 2371091 반응식
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[CH:10]([NH2:12])=[O:11].C(O)=O>O>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH:12][CH:10]=[O:11])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1264-HydroxybenzaldehydeHCID 284Formic AcidHCID 713Formamide

생성물 1

HCID 44371268N-[(4-Hydroxyphenyl)methyl]formamide수율 77.4%

시약·촉매·용매 1

HCID 962Water용매

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온도
189 °C

실험 절차

4-hydroxybenzaldehyde (1.22 g or 10 mmol), formamide (22.72 g or 20.03 mL) and formic acid (2.43 g or 2 mL) were placed into a 50 mL round bottom flask equipped with a thermometer, a reflux condenser, a magnetic stirrer and a heating mantle. The reaction mixture was heated to 189° C. The heating was immediately turned off; the reaction flask was quickly raised from the heating mantle and allowed to cool to room temperature. The TLC conducted on the cold reaction mixture confirmed that the reaction was complete. The reaction mixture was diluted with 50 ml of water and extracted with ethyl acetate. The extract was dried with sodium sulfate and the solvent was evaporated to produce 1.17 g (77.1%) of 4-hydroxybenzylformamide (IV).

후처리

  1. customequipped with a thermometer, a reflux condenser, a magnetic stirrer
  2. temperaturethe reaction flask was quickly raised from the heating mantle
  3. temperatureto cool to room temperature
  4. customThe TLC conducted on the cold reaction mixture
  5. extractionextracted with ethyl acetate
  6. dry with materialThe extract was dried with sodium sulfate
  7. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-2e93053d251a43d9ad171f543479c15f
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08710268B2

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