Propanal → Diethyl 2-(propylamino)malonate

HRID 327434

反応式

HRID 327434 の反応式
[NH2:1][CH:2]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[C:3]([O:5][CH2:6][CH3:7])=[O:4].[O-]CC.[Na+].[CH:17](=O)[CH2:18][CH3:19].C([BH3-])#N.[Na+]>C(O)C>[CH2:17]([NH:1][CH:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])[C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:18][CH3:19]

参加物

6

反応物 4

HCID 527Propanal2 回HCID 81272Propanedioic acid, 2-amino-, 1,3-diethyl esterHCID 2723922Sodium ethoxideHCID 5003444Sodium cyanoborohydride2 回

生成物 1

HCID 15122388Diethyl 2-(propylamino)malonate収率 115.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

Diethyl aminomalonate (21.1 g, 0.1 mol) was dissolved in ethanol and sodium ethoxide in ethanol (50 mL of 1 M) was added. Propionaldehyde (6.6 g, 0.11 mol) and sodium cyanoborohydride (3.6 g, 0.058 mol) were added to the stirred solution. After 30 minutes additional propionaldehyde (6.0 g) and sodium cyanoborohydride (2.6 g) were added to complete the reaction. The solution was evaporated, and the residue was partitioned between ethyl acetate and water. Evaporation of the ethyl acetate gave 25.1 g of diethyl (propylamino)malonate. This was mixed with di t-butyl dicarbonate (34 g, 0.156 mol) and the mixture was heated at 100° C. for 1 hour. The crude product was chromatographed on silica gel using ethyl acetate:hexane as the eluant to give 21.2 g of diethyl (N-(1,1-dimethylethoxycarbonyl)propylamino)malonate as an oil.

後処理

  1. customthe reaction
  2. customThe solution was evaporated
  3. customthe residue was partitioned between ethyl acetate and water
  4. customEvaporation of the ethyl acetate

出典と根拠

ORDレコード
ord-35f630e260f24b428d85bf7fb1e5a8d5
出典データセット
uspto-grants-1993_12
特許番号
US05273975

関連ノート

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