反応式
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:10](OCC)=[O:11]>>[CH2:8]([NH:9][CH:10]=[O:11])[CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
3
反応条件
- 温度
- 50 °C
実験手順
Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 2-phenylethanamine (1.9 g, 15.70 mmol, 1.00 equiv). This was followed by the addition of ethyl formate (5 g, 67.57 mmol, 4.30 equiv) dropwise with stiffing. The resulting solution was stirred overnight at 50° C. The resulting solution was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (70:1). This resulted in 2.27 g (97%) of N-phenethylformamide as yellow oil.
後処理
- customInto a 100-mL 3-necked round-bottom flask purged
- temperaturemaintained with an inert atmosphere of nitrogen
- concentrationThe resulting solution was concentrated under vacuum
- customThis resulted in 2.27 g (97%) of N-phenethylformamide as yellow oil
出典と根拠
- ORDレコード
- ord-3297cd83d6744d5c9fce381b2a37e689
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09193693B2
関連ノート
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