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Pentylamine → 2-Pentylamino-3-methoxypropionaldehyde

HRID 2083602
ノート
印刷プレビュー

反応式

HRID 2083602 の反応式
Cl[CH:2]([CH2:5][O:6][CH3:7])[CH:3]=[O:4].[CH2:8]([NH2:13])[CH2:9][CH2:10][CH2:11][CH3:12]>C1(C)C=CC=CC=1>[CH2:8]([NH:13][CH:2]([CH2:5][O:6][CH3:7])[CH:3]=[O:4])[CH2:9][CH2:10][CH2:11][CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 8060PentylamineHCID 145297052-Chloro-3-methoxypropionaldehyde

生成物 1

HCID 203570052-Pentylamino-3-methoxypropionaldehyde

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

The dimethyl acetal of 2-chloro-3-methoxypropionaldehyde (0.1 mole) and toluene (75 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. Pentylamine (0.22 mole) is added to the reaction mixture with stirring at room temperature. Stirring is continued for a period of about 15 minutes. After this time the reaction mixture is heated at reflux for a period of about 1 hour. The reaction mixture is then cooled to room temperature and filtered. The filtrate is stripped of toluene and unreacted starting material under reduced pressure to yield the desired product the dimethyl acetal of 2-pentylamino-3-methoxypropionaldehyde as the residue.

後処理

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. stirringStirring
  4. temperatureAfter this time the reaction mixture is heated
  5. temperatureat reflux for a period of about 1 hour
  6. temperatureThe reaction mixture is then cooled to room temperature
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-2e9eb048e77d409d9fc443fd9e2f7d26
出典データセット
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04086238

反応ノート

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