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

HRID 2193969
ノート
印刷プレビュー

反応式

HRID 2193969 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1264-HydroxybenzaldehydeHCID 284Formic AcidHCID 713Formamide

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
189 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-9bfa2bc845534aa68410a7d8228650ab
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08329948B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート